Hill-Rom PRO+ 36" MRS Surface — Class II medical device recall Z-1400-2024
Ongoing recall by Baxter Healthcare Corporation, reported 2024-04-10, distributed nationwide. Inconsistencies were identified with service records associated with corrections performed for a previous Medi
| Recall number | Z-1400-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Baxter Healthcare Corporation, Deerfield, IL, United States |
| Recall initiated | 2024-03-05 |
| Classified | 2024-03-29 |
| Reported by FDA | 2024-04-10 |
| Distributed | Nationwide (US) |
| Quantity | 232 units |
| UPC / GTIN / UDI-DI | 00887761977884 |
| Serial numbers | W330BP6363, W330BP6365, W330BP6366, W330BP6367, W330BP6368, W330BP6382, W330BP6383, W330BP6385, W330BP6387, W330BP6397, W333BP6399, W333BP6400, W333BP6401, W333BP6404, W333BP6405, W333BP6406, W333BP6415, W333BP6418, W333BP6420, W333BP6421, W333BP6422, W333BP6423, W333BP6424, W333BP6425, W333BP6426 and 207 more |
| Model numbers | P7924A03 |
Product
Hill-Rom PRO+ 36" MRS Surface, REF P7924A03, The pro+ mattress is intended for patient support and for the prevention and/or treatment of pressure injuries.
Reason for recall
Inconsistencies were identified with service records associated with corrections performed for a previous Medical Device Correction issued by Baxter (ref number: FA-2022-026). Your devices have been identified as potentially impacted by these service inconsistencies and therefore, Baxter will need to reassess the impacted mattresses to confirm they have been corrected as identified by the service order, and to confirm the correct serial numbers have been identified.
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-1400-2024. 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.