HoverMatt — Class II medical device recall Z-2394-2023
Ongoing recall by Stryker Sustainability Solutions, reported 2023-08-16, distributed in AZ, CA, FL, GA, HI, ID, IL, MA…. 39-inche-wide inflatable air transfer mattress packages contain 34-Inch-wide mattresses, so there may be a dec
| Recall number | Z-2394-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Stryker Sustainability Solutions, Tempe, AZ, United States |
| Recall initiated | 2023-06-21 |
| Classified | 2023-08-10 |
| Reported by FDA | 2023-08-16 |
| Distributed | AZ, CA, FL, GA, HI, ID, IL, MA, MD, RI, WI |
| Quantity | 340 |
| UPC / GTIN / UDI-DI | 07613327487718 |
| Lot numbers | 0000185127 |
| Model numbers | HM39SPU-B |
Product
HoverMatt, 39" W x 78" L, REF: HM39SPU-B
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2394-2023. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.