# FDA recall Z-2151-2024

> **Baxter Healthcare Corporation** · Class II · device recall initiated 2024-05-08.

## Product

Centrella Max - The Centrella Smart+ Bed is intended for use in healthcare environments as a patient support system to prevent and/or treat pressure injuries.Multiple model numbers of Centrella Max mattresses and pro+ mattresses.    (1) Centrella Max Surface, REF P7922A01;  (2) Centrella Max Surface, REF P7922A02;  (3) Centrella Max Surface with X-Ray, REF P7922A03;  (4) Centrella Max,Narrow, Rental, REF P7922ARENT01;  (5) Centrella Pro+ 36" Surface with X-Ray, REF P7923A01;  (6) Centrella Pro+ 40" Surface with X-Ray, REF P7923A02;  (7) Centrella Pro+36" Surface, REF P7923A03;  (8) Centrella Pro+ 40" Surface, REF P7923A04;  (9)  Pro+ MRS Surface for Hillrom 900 with X-Ray, REF P006800A01;  (10) 80" MRS with X-Ray AU/NZ  REF P006800A03;  (11) Pro+ MRS Surface for Versacare with X-Ray, REF P3255A01;  (12) Pro+ MRS Surface for Versacare, REF P3255A02;  (13) Pro + MRS Surface for Versacare with X-Ray, REF P3255ARENT01;  (14) Pro+ 36"MRS Surface with X-Ray, REF  P7924A01;  (15) Pro+ 40" MRS

## Reason for recall

There is a potential for the top cover of the hospital bed mattress to delaminate as a result of improper cleaning and lack of adequate details on the appropriate use of cleaning agents containing bleach.

## Distribution

Distribution was made nationwide.  There was also government/military distribution.  Foreign distribution was made to Australia, Canada, China, Japan, Qatar, Saudi Arabia, Singapore, Taiwan, Turkey, and United Arab Emirates.

## Key facts

- **Recall number:** Z-2151-2024
- **Recalling firm:** Baxter Healthcare Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-05-08
- **Report date:** 2024-06-26

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Deerfield, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2151-2024

## Citation

> AI Analytics. FDA recall Z-2151-2024. Retrieved 2026-09-03 from https://api.ai-analytics.org/recall/Z-2151-2024. Source: US FDA. Licensed CC0.

---

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