CLASS II Device recall · Reported 16 Mar 2016 · FDA Enforcement Report

Stryker Position Pro Mattress recalled by Stryker Medical Division of

Stryker Medical Division of Stryker is recalling Stryker Position Pro Mattress, distributed nationwide in the US. The recall was initiated on 3 Dec 2015 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesmodel number: 2920-000-000 units serialized

Quantity recalled2694

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number: Z-1081-2016
FDA event ID: 72935
Recalling firm: Stryker Medical Division of Stryker, Portage, MI
Classification: Class II
Status: Terminated
Recall initiated: 3 Dec 2015
FDA classified: 8 Mar 2016
Reported: 16 Mar 2016
Type: Voluntary: Firm initiated
Customers notified by: Letter
Reason category: Other Reasons
Device type: Other Medical Devices

Timeline

3 Dec 2015	Recall initiated by company
8 Mar 2016	Classified by FDA	+96 days
16 Mar 2016	Published in enforcement report	+8 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Potential for power cord to melt; hazards include electric shock and fire.

Product as listed by the FDA

Stryker Position Pro Mattress. Mattress, Air Flotation, Alternating Pressure. PositionPRO is a powered pressure relief support surface with low air loss (LAL) intended for medical purposes. PositionPRO consists of multiple air cells filled and emptied by an integrated control unit to provide changes in the distribution of body weight for pressure relief. PositionPRO offers turn assist. PositionPRO is for use with GoBed II¿, Secure II/3¿, InTouch¿, and Epic II¿ 84 in. x 35 in. flat deck frames. This surface is powered via an AC power cord that comes in either a 4 foot long option (PN QDF8087) or 15 foot long option (PN QDF8088). The 4 foot long option is used when the surface is plugged into the auxiliary outlet of the bed. The 15 foot long option is utilized when the surface needs to be plugged into a wall outlet. This product uses a power cord, manufactured by ElectriCord that plugs into the wall outlet or the auxiliary outlet of the bed that the surface is placed onto.

Where it was distributed

Worldwide Distribution - US Nationwide and the countries of Brazil, Canada, Chile, France, Hong Kong, Italy, Mexico, South Korea, Switzerland, United Kingdom.

Nationwide

Questions about this recall

Is Stryker Position Pro Mattress recalled?

Yes. Stryker Medical Division of Stryker recalled Stryker Position Pro Mattress on 3 Dec 2015. The recall is Class II and its status is Terminated. Recall number Z-1081-2016.

Why was it recalled?

Potential for power cord to melt; hazards include electric shock and fire.

Which lots are affected?

model number: 2920-000-000 units serialized

Where was it sold?

Worldwide Distribution - US Nationwide and the countries of Brazil, Canada, Chile, France, Hong Kong, Italy, Mexico, South Korea, Switzerland, United Kingdom.

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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