FDA Device recall Z-2394-2023
HoverMatt, 39" W x 78" L, REF: HM39SPU-B
- FDA Device
- Class II
- ongoing
- Published 2023-08-16
On 2023-08-16 the FDA classified a Class II recall of HoverMatt, 39" W x 78" L, REF: HM39SPU-B by Stryker Sustainability Solutions, citing 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 acro….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2394-2023 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-06-21 |
| Published | 2023-08-16 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Stryker Sustainability Solutions |
| Distribution | AZ, CA, FL, GA, HI, ID, IL, MA, MD, RI, WI |
Product
HoverMatt, 39" W x 78" L, REF: HM39SPU-B
Reason
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.
Identifiers
| code_info | UDI-DI: 07613327487718, Lot: 0000185127, Distribution Dates: 11/28/2022-12/08/2022 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2394-2023%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.