Stryker Sustainability Solutions: Medical Device Recall in 2023 - (Recall #: Z-2394-2023)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

HoverMatt, 39" W x 78" L, REF: HM39SPU-B

Product Classification:

Class II

Date Initiated: June 21, 2023

Date Posted: August 16, 2023

Recall Number: Z-2394-2023

Event ID: 92655

Reason for Recall:

39-inche-wide inflatable air transfer mattress packages contain 34-Inch-wide mattresses, so there may be a decreased surface area available to distribute the patient's weight across, which may increase the effort exerted by staff for a lateral patient transfer, and there may be increased friction and shearing forces when the patient is moved resulting in skin tear injury.

Status: Ongoing

Product Quantity: 340

Code Information:

UDI-DI: 07613327487718, Lot: 0000185127, Distribution Dates: 11/28/2022-12/08/2022

Distribution Pattern:

US: WI, ID, CA, FL, HI, MD, RI, AZ, MA, GA, IL

Voluntary or Mandated:

Voluntary: Firm initiated