Hill-Rom Centrella Pro+ 36" Surface With X-Ray mattress — Class II medical device recall Z-1415-2022
Ongoing recall by Baxter Healthcare Corporation, reported 2022-07-27, distributed nationwide. The failure mode on the affected mattresses can cause a reduction in the performance of the Microclimate Manag
| Recall number | Z-1415-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Baxter Healthcare Corporation, Deerfield, IL, United States |
| Recall initiated | 2022-06-24 |
| Classified | 2022-07-20 |
| Reported by FDA | 2022-07-27 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA |
| Quantity | 136 mattresses |
| UPC / GTIN / UDI-DI | 00887761977945 |
| Serial numbers | W238BP4338, W238BP4339, W238BP4340, W238BP4341, W238BP4342, W238BP4344, W238BP4345, W238BP4347, W238BP4348, W354BP6891, W354BP6892, W354BP6897, W354BP6898, W354BP6899, W354BP6906, W354BP6908, W354BP6909, W354BP6910, W354BP6911, W354BP6916, W354BP6917, W354BP6918, W354BP6919, W354BP6920, W354BP6921 and 111 more |
| Model numbers | P7923A01 |
Product
Hill-Rom Centrella Pro+ 36" Surface With X-Ray mattress, REF P7923A01.
Reason for recall
The failure mode on the affected mattresses can cause a reduction in the performance of the Microclimate Management feature used to pull heat and moisture away from the patient resulting in an increased patient risk of pressure ulcer development.
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-1415-2022. 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.