# FDA recall Z-2394-2023

> **Stryker Sustainability Solutions** · Class II · device recall initiated 2023-06-21.

## 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.

## Distribution

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

## Key facts

- **Recall number:** Z-2394-2023
- **Recalling firm:** Stryker Sustainability Solutions
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-06-21
- **Report date:** 2023-08-16

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Tempe, AZ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2394-2023

## Citation

> AI Analytics. FDA recall Z-2394-2023. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-2394-2023. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*