Stryker Medical Division of Stryker Corporation: Medical Device Recall in 2016 - (Recall #: Z-1081-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

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.

Product Classification:

Class II

Date Initiated: December 3, 2015

Date Posted: March 16, 2016

Recall Number: Z-1081-2016

Event ID: 72935

Reason for Recall:

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

Status: Terminated

Product Quantity: 2694

Code Information:

model number: 2920-000-000 units serialized

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated