Important Notice: The equipment must be
installed and operated in the manner for which it
was intended. Facility staff/user is responsible for
reading and understanding the product user manual
and contacting Joerns Healthcare if anything in this
manual is unclear. Joerns will not be held responsible
for any injuries resulting from failure to comply with
the instructions and precautions in this manual.
Warning: Joerns specialty support surfaces are
designed as mattress replacement systems. The risk
of entrapment may occur when the equipment is
placed on bed frames that leave gaps of even a few
inches between the mattress and the head panel,
foot panel, and bed or side rails. The equipment is
NOT to be used when such gaps are present.
Facility staff/user is responsible for ensuring that all
mattresses properly t the bed frames. Joerns is not
responsible for the placement of its equipment on
bed frames that leave gaps between the mattress
and the head panel, foot panel or bed or side rails
which present a risk of harm to patients.
Warning: An optimal bed system assessment
should be conducted on each patient by a
qualied clinician or medical provider to ensure
maximum safety of the patient. The assessment
should be conducted within the context of, and in
compliance with, the state and federal guidelines
related to the use of restraints and bed system
entrapment guidance, including the Clinical
Guidance for the Assessment and Implementation
of Side Rails published by the Hospital Bed
Safety Workgroup of the U.S. Food and Drug
Administration. Further information can be obtained
at the following web address: http://www.fda.gov/
MedicalDevices/ProductsandMedicalProcedures/
GeneralHospitalDevicesandSupplies/HospitalBeds/
default.htm.
When using the mattress system, always ensure that
the patient is positioned properly within the connes
of the bed. Do not let any extremities protrude over
the side or between the bed rails when the mattress
is being used.
Danger Explosion Hazard: Do not use in the
presence of ammable anesthetics. Do not use in
the presence of smoking materials or open ame.
Air owing through the air mattress will support
combustion.
Warning: A possible re hazard exists. This product
is suitable for use with oxygen administering
equipment of the nasal, mask, or half bed-length,
tent-type only. To prevent personal injury or
equipment damage, ensure that the oxygen tent
does not extend below the mattress.
Danger: To reduce the risk of shock, adhere to the
following instructions. Failure to do so could result in
personal injury or equipment damage.
• Immediately after using the TurnCair Therapeutic
Support System, unplug it from its power source.
• Do not place or store the product where it can fall
or be pulled into a tub or sink.
• Do not place or drop the product into water or
other liquid.
• Do not remove the back of the control unit. Refer
servicing to Joerns.
Warning: To reduce the risk of burns, shock, re, or
personal injury, adhere to the following instructions.
Failure to do so could result in personal injury or
equipment damage.
1. Use this product only for its intended purpose as
described in this manual. Only use attachments
and/or accessories that are recommended by the
manufacturer.
2. If this product has a damaged power cord or
plug, is not working properly, has been dropped
or damaged, or has been dropped into water, do
not operate it. For examination and repair, return
the product to Joerns.
3. Keep the control unit and power cord away from
heated surfaces, e.g. space heaters.
4. Never block the air openings of the product. Do
not place the control unit on a surface, such as a
bed or couch, where the air opening and/or lter
compartment, located on the back of the control
unit, may be blocked. Keep the air openings free
of lint and hair.
5. Never drop or insert any object into any opening
or hose.
6. Do not spill food or liquids onto the control
unit. If a spillage does occur, turn off the unit,
disconnect it from its power supply and allow at
least 24 hours for drying.
7. Do not use the product outdoors, or where
aerosol-spray products are used.
8. Plug this product only into a properly grounded
outlet. Refer to “Grounding Instructions”.
9. Ensure nothing is placed on the power cord and
ensure it is not located where it can be stepped
on or tripped over.
10. Do not attempt to service the control unit. Please
call Joerns for any service requests.
11. The therapy pad (top cover) of this product is
not air permeable and may present a suffocation
risk. It is the responsibility of the caregiver to
ensure that the patient can use this product
safely.
Page 3
Joerns Therapeutic Support Surfaces
TurnCair
Save These Instructions for Future Reference
Bed System Entrapment Information
In April 1999, the U.S. Food and Drug Administration
(FDA) in partnership with representatives from
the hospital and post-acute bed industry, including
Joerns Healthcare, national healthcare organizations,
resident advocacy groups, and other federal agencies
formed the Hospital Bed Safety Workgroup (HBSW).
The workgroup’s goal is to improve the safety of
bed frames for residents and patients in all health
care settings who are most vulnerable to the risk of
entrapment. The efforts of the FDA and the HBSW
culminated in the FDA’s release of recommended
guidelines intended to reduce the risk of entrapment,
including dimensional limits for critical gaps and
spaces between bed system components and clinical
guidance for assessment and implementation of bed
side rails in various health care settings.
Entrapment zones involve the relationship of
bed components often directly assembled by the
healthcare facility rather than the manufacturer.
Therefore, compliance is the responsibility of the
facility.
Creating a Safer Care Environment
While the guidelines apply to all healthcare settings
(hospitals, nursing homes and home care), longterm care facilities have particular exposure since
serious entrapment events typically involve frail,
elderly or dementia residents.
For More Information
To learn more about compliance options
with Joerns products, visit our website at
www.joerns.com, or contact our Customer Care
representatives at 800.826.0270 and ask for free
informational publications.
To learn more about entrapment zones,
assessment methods, and guidelines concerning
entrapment, contact Joerns at 800.826.0270 or
consult the FDA website: http://www.fda.gov/
MedicalDevices/ProductsandMedicalProcedures/
GeneralHospitalDevicesandSupplies/HospitalBeds/
default.htm.
As the leading manufacturer of long-term care beds
and a frontrunner in addressing this critical issue,
Joerns can offer you the expertise, assistance and
products to bring your facility into compliance.
Joerns® Compliance Solutions
Matching the right bed components in order to meet
regulatory guidelines can be complex.
That is why Joerns offers a wide array of compliance
options. We assist customers in selecting compliant
Features ...............................................................................................................................................6
Therapy Control Unit Features
Therapy Mattress System Features
Therapy Pads
Additional Features ..............................................................................................................................7
The TurnCair, provided by Joerns Healthcare, is
a unique, continuous bilateral rotation mattress
replacement system. This system is designed
to meet pressure redistribution and rotational
therapy needs of patients with pressure ulcers,
special respiratory needs, and those at risk of
skin breakdown. Low air loss therapy has been
demonstrated to reduce the risk of pressure ulcers.
Warning: The risk of entrapment can arise when
equipment is placed on bed frames that leave gaps
of even a few inches between the mattress and the
headboard, footboard, and bed or side rails.
The equipment is NOT to be used when such gaps
are present. See “Important Precautions” section of
this manual.
The TurnCair mattress replacement system is
suitable for both the treatment of existing pressure
ulcers stage I through stage IV as well as those who
have been assessed at risk from the complications
of immobility. The TurnCair is quiet, comfortable
and simple enough for single caregiver installation,
featuring rapid ination in just three to ve minutes.
The user-friendly controls allow for easy adjustment
of patient comfort.
Additionally, low friction and low shear materials,
together with average interface pressures well below
capillary closure levels (32mm of Mercury), means
that the TurnCair meets the comfort and clinical
requirements of your patients.
Moisture Control
Patients are at risk for skin maceration if excess
moisture is permitted to accumulate beneath
the patient. This may be due to perspiration,
incontinence or wound drainage.
coated nylon therapy pad. The moisture vapor
permeable fabric of the therapy pad allows a
sufcient amount of air to circulate beneath the pad
and wicks away excess moisture.
Shear and Friction Reduction
Shearing occurs when the skin is stationary in
relation to the support surface, while the underlying
tissues and vessels are stretched and damaged.
When a patient’s skin rubs against another surface,
the result is friction. The top surface of the TurnCair
therapy pad is constructed from a very smooth nylon
fabric with low friction and low shear properties
to protect the patient’s skin from these damaging
forces.
Indications for Use
Note: The selection of a pressure-redistributing
surface needs to be based on each individual
patient’s clinical condition, diagnosis and/or comorbidities. The choice and use of a support surface
is one factor in a holistic program of wound care and
treatment.
We have ensured that the TurnCair addresses the
four key areas in the treatment of compromised
skin: pressure redistribution, moisture control, and
reduction in both friction and shearing forces.
Pressure Redistribution
The TurnCair is divided into three distinct anatomical
zones: head, torso and foot. Each zone is adjusted to
ensure optimal pressure redistribution and provide a
comfortable sleeping surface.
The TurnCair provides maximum pressure
redistribution through delivering a specic amount
of air to each therapy cell and allowing controlled
amounts of air to escape, thus equalizing the
pressure between the patient and the therapy cells.
This distributes the patient’s weight evenly over a
large surface area resulting in pressure readings well
below capillary closure levels.
Spinal Cord Injury
The TurnCair is not recommended for use by patients
with unstable spinal fractures. Advice should be
obtained from the appropriate physician before
using the TurnCair system for these patients.
The TurnCair provides uniform distribution of weight
over a wide surface area, which redistributes
pressure against bony prominences and provides a
soft, gentle therapy surface to lie on. For patients
experiencing severe pain and discomfort due to
pressure and/or positioning limitations, consider
the TurnCair as an adjunct to pain management
interventions.
Note: Pressure redistribution and pain management
are conditions and diagnoses for which the TurnCair
may be indicated. Occasionally, there are orthopedic
and neurological patients that require body
positioning to be maintained in specic alignment.
The TurnCair has safety features and a therapy
support cell to prevent deation of the therapy
cells and to keep patients in otation at all times.
However, in the event of error or malfunction,
the therapy cells may deate and not provide the
necessary alignment. The use of the TurnCair for
these patients should be considered on an individual
basis and discussed with the attending physician.
Respiratory Relief
Conditions associated with acute respiratory failure
The TurnCair provides lateral rotation therapy for
patients suffering from various types of respiratory
failure. The rotation helps promote pulmonary
drainage and is appropriate for patients who require
mechanical ventilation.
Features
The TurnCair is comprised of two components:
Therapy Mattress System Features
• Twenty individual therapy cells help to evenly
distribute the patient’s weight and maximize
pressure redistribution.
• Modular cell design mattress for ease of cleaning,
re-assembly and cost effective service.
• Lower two-inch therapy support cell provides
additional therapeutic support and remains inated
for up to 12 hours in the event of a power failure.
• Lower mattress therapy enclosure provides for
stable ingress and egress and reduces entrapment
concerns
• Eight-inch deep therapy cells are constructed
of highly durable, polyurethane coated nylon to
provide adequate support and prevent bottoming
out for most patients within weight limit.
• Side bolsters support patient during rotation
• Durable base tub is constructed from 100% heavy
weight 1680 denier nylon with a 1.5 oz. urethane
coating and incorporates bed attachment loops for
stability.
• Maximum weight capacity of 400 lbs.*
• Quick CPR deation in 30 seconds or less
• Anti-kink, easy clean air supply hose set
Therapy Pads
• Therapy control unit
• Therapy mattress system
Therapy Control Unit Features
• Turn Time set options of 10, 20, 30 and 60
minutes- 60 minutes is also hold angle function
• Turn Angle options of ¼, ½, ¾ and Full
• Turn option settings: Left, Right, Dual, or None
• True low air loss with up to 100 liters of airow per
minute
• Three modes of operation – Autorm, Turn and
Static
• Autorm mode provides maximum air ination
designed to assist both patients and caregivers
during patient transfer and treatment
• Automatic panel lockout to avoid unwanted or
accidental adjustments
• Eight therapeutic comfort control settings to
maximize patient compliance and promote healing
• Closed loop pressure sensor control system
eliminates concerns of changes in mattress
interface pressure due to ambient temperature and
pressure changes.
• Integrated swing out hanging brackets for xing to
most bed frames
• Crisp, easy to read graphics for intuitive set up and
therapy control
• Quick disconnect hose feature allows for rapid
attach and CPR deate at the control unit
• Audible and visual alarms for power interruptions
• Compact lightweight control unit is quiet, robust
and powerful, with a reusable air lter and
Many healthcare facilities are facing the challenge of
infection control. Joerns’ quilted therapy covers are
treated with an antimicrobial to protect the therapy
pad itself from the growth of mold, mildew and odorcausing bacteria.
Key Features and Benets:
• Treated with a highly effective bacteriostat agent
to inhibit the growth of bacterial and fungus
• Constructed from a very smooth nylon fabric with
low friction and low shear properties to protect
the patient’s skin from damaging friction/shearing
forces
• Breathable, moisture vapor permeable fabric allows
air to circulate beneath the pad and wicks away
excess moisture. This keeps your patient dry and
helps to prevent skin maceration. A unique feature
of the therapy pad is that it
• Two-way stretch therapy pad is designed for
optimal comfort, moisture vapor transfer, stain
resistance and ease of laundering
Additional Features
CPR
The hose connection at the control unit is marked
CPR. Disconnect the hose from the control unit.
Deation times will vary based on patient weight and
prole. To resume therapy, reattach the hose to the
control unit.
Page 7
Joerns Therapeutic Support Surfaces
TurnCair
Transport
To transport the patient in bed, turn the control unit
off. Unplug the power cord from the outlet. Do not
disconnect the hose connection at the control unit.
The lower support cell will prevent the patient from
bottoming out for up to 12 hours.
Power Failure
After a power failure the unit will start up in standby
mode. Reset the preferred mode and comfort level as
described in the “Keyboard Functions” section. In the
event of a power failure the lower support cells will
hold air for up to 12 hours. In case of an extended
power failure, transfer the patient to a hospital
mattress or other surface.
Optional Accessories
• Additional therapy pads – available for purchase.
Keyboard Functions
Warning: For important precautions, see page two.
Caution: The patient’s head should be positioned in
the center of the top section of the mattress. When
using the mattress system always ensure that the
patient is positioned properly within the connes of
the bed. Do not let any extremities protrude over the
side or between the bed rails when the mattress is
being used.
Power Button
Use the Power button to turn the power on and off.
Hold
The Hold feature is used to immediately stop all
rotation and hold the current mattress position. The
mattress will hold this position until this feature is
turned off by pressing the Hold button a second
time.
Autorm
Autorm mode provides maximum air ination
designed to assist both patients and caregivers
during patient transfer and treatment. The unit
will automatically return to the mode it was in
prior to Autorm (either Therapy or Pulsate) in
approximately 12 minutes.
Turn
The Turn function places the system in the Turning
mode. Use this button to select the type of rotation
desired for the patient. The mattress can be turned
to only the left or right side or to both sides in
sequence. The None position will turn off the Turn
mode.
Turn Time
Sets Turn Time options of 10, 20, 30 and 60
minutes. Sixty minutes is also a Hold angle function.
When this LED is blinking, it indicates that the
mattress is being held in its current position. To
resume turning, press the Turn Time button until the
desired cycle time is selected.
Turn Angle
Sets Turn Angle options of 1/4, 1/2, 3/4 and Full.
Full is the maximum turn angle and approximates
a 30 degree turn angle for patients with lighter
body weight and narrow body shape– other patient
weights and body shapes will result in different turn
angles.
Comfort Adjust
The Comfort Adjust function is located on the right
side of the control panel. The TurnCair can be
customized to meet individual patient needs within
a therapeutic window. Use the up and down keys to
simultaneously increase or decrease pressure in all
three zones (head, seat and foot). This function will
not work in Autorm mode.
Lockout
Note: The unit is designed to lock out all the
adjustment controls after the patient has been
positioned correctly. In approximately ve minutes
after the last button push the power on light begins
to ash indicating Lockout is enabled. This feature is
to prevent any unauthorized changes to the patient
settings.
To unlock and make adjustments to the settings
press both up and down comfort arrows at the same
time to disengage the Lockout function. The lockout
function will return in approximately ve minutes.
The TurnCair has two therapy modes:
• Turn: The Turn mode provides a continuous
rotation cycle on selected times and at selected
angles
• Static: The unit starts in the Static mode, which is
the standard low air loss therapy.
Warning: Use a properly grounded, three-prong,
120V AC outlet for this product. Failure to use a
grounded outlet could result in personal injury or
damage to equipment or house wiring, including risk
of re. A qualied electrician should be contacted to
correct the wiring and ensure a properly grounded
outlet.
Before installing this product, have the electrical
system checked to make sure the electrical circuits
and the electrical service are properly grounded.
Having a three-prong outlet does not necessarily
mean it is grounded. Sometimes two-prong outlets
are replaced with a three-prong type even though
there is no ground wire.
There is always a chance of a loose connection or
poor installation of a ground wire that causes the
loss of proper ground at the outlet. Inadequate
grounding at electrical outlets can occur even if there
is a ground wire. Wires can become loose over time
at the connection to the outlet.
Note: To install new wires on a circuit requires a
qualied electrician.
How to Determine if Your Outlet has the
Proper Grounding
Most hardware stores sell circuit testers (Figure
1) that can be used to test an outlet for proper
grounding. The tester plugs into an outlet and by
observing the indicator lights you can determine if
the outlet is properly grounded. For a higher level
of assurance, an electrician should be requested
to thoroughly test the electrical system with more
reliable equipment.
If repair or replacement of the cord or plug is
necessary, please contact Joerns Healthcare for
assistance.
Figure 1
Setup
Warning: For important precautions, see page two.
Caution: Do not place the control unit on the oor.
Position the power cord to keep personnel from
tripping over it.
Note: The TurnCair system must be installed on bed
frames that are equipped with side rails. Please raise
side rails on the bed and lock them in position after
the patient is on the mattress. Never leave patient
unattended on mattress system with bed side
rails in the down position.
When the product is not in use, properly store the
power cord. Failure to do so could result in personal
injury.
• Remove the existing mattress from the bed.
• Unroll the mattress with the hose connection at the
foot end of the bed and the therapy cells facing up.
Secure the straps on the mattress to the movable
part of the bed frame.
• If the therapy pad is not already on the mattress,
place it on the mattress. Attach the elastic straps
to the mattress buckles around each corner of
the mattress. Attach the additional straps to the
movable part of the bed frame.
• Hang the control unit on the foot of the bed facing
away from the bed. Attach the hose connector
marked CPR to the control unit.
• Plug in the control unit and the orange Standby
light will illuminate. Press the Power button. The
control unit will start and the green light will
illuminate. Keep the control unit ON while the
patient is on the mattress.
• Fully inate the mattress by selecting Autorm.
When the mattress is fully inated, select the
Therapy mode, and place the patient on the
mattress. Note: Keep the control unit on while the
patient is on the mattress.
• Select the appropriate Comfort Adjust level to
prevent bottoming out (i.e. providing greater
than one inch of air between the patient’s sacral
area/buttocks and the lower safety mattress) as
outlined:
1. Begin by placing the head of the bed in the
appropriate position based on the patient’s
clinical condition.
2. Select the highest or most rm Comfort Adjust
setting.
3. Hand Check: Place a hand with three (3) ngers
(if head of bed at 30° or higher) or four (4)
ngers (if head of bed lower than 30°) stacked
vertically beneath the cells of the mattress and
above the safety mattress directly between
the lowest point of the patient’s sacral area/
to the rmness level where the height of the
three (3) or four (4) ngers can slide with
minimal resistance between the patient’s sacral
area/buttocks and the lower safety mattress.
This is the proper Comfort Adjust setting for the
patient to assure proper ination of the air cells
and prevent bottoming out of the mattress.
5. Document the patient’s Comfort Adjust setting
for future reference, and re-evaluate with the
hand check as the patient’s condition warrants.
6. The safety side bolsters cannot be inated unless
the CPR plug is installed. The plug is located on
the hose assembly between the mattress and the
control unit.
Caution: The safety side bolsters should always be
inated when patient is unattended on the mattress
and/or the mattress is in turn mode.
Troubleshooting
Therapy Surface is Not Inating
1. Ensure the hose connection from the therapy
mattress system (mattress) to the control unit is
securely connected.
2. Ensure that the control unit is plugged into an AC
outlet.
3. Ensure that the power is not on Standby. If on
Standby, press the Power button.
4. Ensure that all air cells are connected to the
manifold.
Unable to Change Therapy Mode or Adjust
Comfort Control
Make sure the Lockout function is disabled. To
disable, press the up and down comfort adjust
arrows simultaneously.
Nursing Procedures
Recommended Linen:
Special linens are not necessary for the TurnCair.
While there is no need for a bottom sheet the
therapy pad should be covering the therapy cells at
all times. The patient should never be lying directly
on the therapy cells. Upon the patient specic needs
the following linens may be utilized:
• Draw or slide sheet to aid in positioning and to
further minimize friction and shearing
• Incontinence barrier pad for patients incontinent
of urine and/or stool, and patients with heavily
draining wounds
• Add top sheet, blanket and/or bedspread as
needed for patient comfort
• Keep the amount of padding between the patient
and bed to a minimum for optimum performance
Changing the Therapy Pad
1. Place the therapy pad over the therapy cells,
tting the corner of the cushions into the corner
of the therapy pad. (Similar to a tted sheet)
2. Zip the therapy pad along each side of the
mattress tub.
Patient Positioning and Comfort
General Repositioning
Patients should be turned and repositioned per
individual turning schedule or per facility policy. It
may be helpful to activate the Autorm mode to
achieve a rm surface for repositioning purposes.
The unit will automatically return to the mode it was
in prior to Autorm in approximately 12 minutes
or you can manually return to therapy mode once
patient has been repositioned.
Unless counter indicated, it is desirable to keep
the head of the bed in the low position to provide
optimal pressure redistribution and minimize the risk
of shearing injuries.
Elevating Patient into Sitting Position
The special properties of the TurnCair, therapy pad
reduce the opportunity for shear and friction that
may occur when raising the back section of other
beds. As with any surface, sliding can be expected,
therefore patients should be repositioned after
elevation. The knee gatch or knee section of the bed
may be elevated rst, to help prevent the patient
from sliding when the back section of the bed is
elevated.
Incontinence
Moisture against the skin surface leads to
maceration, or softening of the tissues. To prevent
maceration, we recommend you use an incontinence
barrier pad to absorb the excess moisture.
In the event of incontinence or excess drainage on
the therapy pad, you should wipe off the excess uid
from the bed surface.
Safety Information
Patient Migration
Specialty bed products are designed to reduce/
redistribute pressure and the shearing/friction
forces on the patient’s skin. The risk of gradual
movement and/or sinking into hazardous positions
of entrapment and/or inadvertent bed exit may be
increased due to the nature of these products.
With any traction or unstable fractures, maintain
physician-directed angle of articulation and guard
against risks of patient migration or inadvertent
deation of patient surface.
Skin Care
Monitor skin conditions regularly, particularly in areas
where incontinence and drainage occur or collect,
and consider adjunct or alternative therapies for high
acuity patients. Early intervention may be essential
to preventing serious skin breakdown.
Bed Height
To minimize the risks of falls or injury the patient
surface should always be in the lowest practical
position when the patient is unattended. Make sure
areas under and around the frame are clear of
objects, persons and parts of body before
adjusting height.
Cleaning
Warning: Unplug the control unit from its power
source. Failure to do so could result in personal
injury or equipment damage.
Warning: Do not expose the unit to excessive
moisture that would allow for liquid pooling. Personal
injury or equipment damage could occur.
Caution: Do not use harsh cleansers/detergents,
such as scouring pads and heavy-duty grease
removers, or solvents, such as acetone. Equipment
damage could occur.
Control Unit
Wipe off dust. If necessary, clean the housing
exterior with a disinfectant solution or a mild
detergent and a damp cloth. Then wipe dry.
1. Patient care equipment that does not come in
contact with mucous membranes or non-contact
skin requires low-level disinfection. Wiping
surfaces with a properly prepared detergent or
disinfectant carries out low level disinfecting.
2. Processing of dirty patient care equipment should
take place in a designated area away from clean
or sterile supplies and food preparation areas.
3. Detergent/disinfectants should not be mixed with
other germicides or detergents. Using the proper
dilution insures the most effective killing power
of the disinfectant.
4. Wash hands often and well, including after
removal of gloves.
5. Patient care equipment that is used in isolation
areas should be disinfected in accordance with all
internal policies and procedures regarding such
equipment.
Disinfecting
When there is visible soilage and between patients,
we recommend that you disinfect the unit and
mattress with a tuberculocidal disinfectant.
Disinfectant should be registered with the
Environmental Protection Agency (EPA).
1. Use rubber gloves and eye protection.
2. Prepare detergent/disinfectant (registered by
EPA as hospital disinfectant) solution according
to instructions on label for correct use-dilution.
3. With support surface deated, thoroughly wipe
down entire mattress, as air cells will lie at.
Be sure to reach all areas underneath and inbetween air cells. Allow to air dry.
4. If dust or other soiling has accumulated along
air hoses, remove using swabs moistened with
detergent/disinfectant as necessary. Allow all
components to air dry. Wrap mattress in plastic
and return to storage area.
5. Thoroughly wipe down outside of control unit and
allow to air dry. Cover with plastic and return to
storage area
6. Remove gloves and dispose; wash hands.
Therapy Pad
General Cleaning
If there is no visible soilage with possible body uids,
we recommend that you clean the mattress system
with a mild detergent and warm water. If disinfection
is desired, you may use a combination cleanser/
disinfectant as explained in “Disinfecting” area.
The therapy pad can be wiped down with a
disinfectant solution or a mild detergent with a
damp cloth. If heavily soiled, the therapy pad can
be laundered in a washer and dryer with warm
water (no more than 120º Fahrenheit). A non-bleach
detergent should be used sparingly. Wipe dry or
allow to air dry.
Steam Cleaning
Do not use any steam cleaning device on the unit.
Excessive moisture can damage mechanisms in this
unit.
Page 11
Joerns Therapeutic Support Surfaces
TurnCair
Filter Cleaning
Check the air lter on the rear of the unit regularly
for buildup of dust/dirt. If buildup is visible turn
off the control unit and disconnect the power cord
from the wall outlet. Remove the lter by grasping
the lter pulling outward. Replace with the second
supplied lter. Ensure the replaced lter covers the
entire lter region.
Hand-wash the removed lter in warm soapy water
and allow to air dry. When dry, store the lter in a
safe place for the next lter maintenance.
Maintenance
Warning: Only facility-authorized personnel trained
by Joerns Healthcare should perform preventative
maintenance. Preventative maintenance performed
by unauthorized personnel could result in personal
injury or equipment damage. Any maintenance
done without Joerns authorization will invalidate any
warranties on this product.
Storage And Care
Note: Clean the TurnCair as described in the
previous section prior to storage.
Control Unit
The power cord may be wrapped around the unit for
convenience. Wrap the unit in a plastic bag for dust
resistance then store the unit in an area appropriate
for an electronic medical device.
Support Surface
System Specications
Weight
Control unit: ............................. 14 lbs ....... (6 Kg)
Mattress: ................................. 24 lbs. .....(11 Kg)
Maximum weight capacity*......... 36"(W) and 42"(W)
36" (91cm) W x 80" (203cm) L x 10" (25cm) D
42" (107 cm) W x 80" (203 cm) L x 10" (25 cm) D
48" (122 cm) W x 80" (203 cm) L x 10" (25 cm) D
*Mattress weight capacity only; total weight must not
exceed bed frame manufactures’ specied load capacity
Electrical Specications
USA
88 -132V AC, 47- 63 Hz, 2A (Startup)
Less than 1A (Running)
European/Australian
176V - 264V AC, 47 - 63 Hz, 1A (Startup)
Less than 0.5A (Running)
Environmental Conditions
Operating Conditions:
Ambient temperature: +10°C to +40°C
Relative humidity: 30% to 75% non-condensing
Gently roll up the support surface, expelling any
residual air, for temporary storage. The mattress
should be wrapped in plastic and/or a clean bag for
storage.
Storage And Shipping Conditions:
Ambient temperature: 10ºC to +40ºC
Relative humidity: 10% to 100%
Control Unit Agency Approvals
• UL Classied: UL 60601-1 CAN/CSA C22.2
No. 60601-1
• UL Classied per Canadian standard: Medical
Electrical Equipment, CSA 601.1 M90
Call For Assistance
If you have any questions or require service on a
Joerns product, please call Joerns Healthcare at
Joerns Healthcare warrants the TurnCair mattress
to be sold free from defects in workmanship and
materials, under normal and proper use, for a
period of two (2) years on the mattress, and one (1)
year on the cover and electromechanical mattress
components (compressors, valves, printed circuit
boards, hoses, and couplers). Damages arising from
improper use will not be covered by this warranty.
Improper use is dened as those caused by:
• Burns
• Use of improper chemical agents
• Needle punctures, cuts or abrasions
• Excessive loads
• Staining
• Negligent or excessive usage
• Improper maintenance, handling and/or cleaning
• Failure to use in the manner indicated in the
TurnCair user manual
Any modication, repair or alteration done to the
TurnCair that were not authorized in writing by
Joerns Healthcare will void this warranty.
Damage caused by use in unsuitable environmental
conditions, abuse or failure to maintain the product
in accordance with user and service instructions is
not covered.
Parts
Joerns Healthcare’s TurnCair contain various parts
that wear from normal use. Joerns Healthcare’s
obligation under this warranty is limited to supplying
replacement parts, servicing or replacing, at its
option, any product which is found by Joerns to be
defective. When requested by Joerns, parts must be
returned for inspection at the customer’s expense.
Credit will be issued only after inspection.
Service
Most service requests can be handled by the facility
Maintenance Department with assistance from the
Joerns Healthcare Product Service Department.
Most parts requested can be shipped next day air at
the customer’s expense.
Should a technician be required, one will be provided
by Joerns Healthcare, at our discretion. Only the
Joerns Healthcare Product Service Department can
dispatch authorized technicians.
This warranty is extended to the original purchaser
of the equipment.
Post Acute, Acute, HomeCare
2430 Whitehall Park Dr. Ste 100
Charlotte, NC 28273
(P) 800.826.0270
(F) 800.457.8827