Recall archive / FDA device enforcement
HoverMatt, 39" W x 78" L, REF: HM39SPU-B — FDA record Z-2394-2023
Reported ongoing
Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.
Source date Jun 21, 2023. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
What the record says
- 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.
- Classification
- Class II
- Recalling firm
- Stryker Sustainability Solutions
- Quantity
- 340
- Agency-reported status
- Ongoing
- Source record identifier
- Z-2394-2023
What the recall classes mean. Classification is an agency assessment, not individual medical advice.
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | UDI-DI: 07613327487718, Lot: 0000185127, Distribution Dates: 11/28/2022-12/08/2022 |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
US: WI, ID, CA, FL, HI, MD, RI, AZ, MA, GA, IL
States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.
Dates in the source
- Report date
- Aug 16, 2023
- Recall initiation date
- Jun 21, 2023
- Center classification date
- Aug 10, 2023
FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.