Hill-Rom pro+ mattress — Class II medical device recall Z-1482-2023
Ongoing recall by Baxter Healthcare Corporation, reported 2023-05-10, distributed nationwide. There is a potential for mattress cover damage (delamination) which may result in fluid absorption in the matt
| Recall number | Z-1482-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Baxter Healthcare Corporation, Deerfield, IL, United States |
| Recall initiated | 2023-03-31 |
| Classified | 2023-05-01 |
| Reported by FDA | 2023-05-10 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA, QA |
| Quantity | 5,549 units |
| UPC / GTIN / UDI-DI | 00887761968110, 00887761976863, 00887761976887, 00887761977839, 00887761977846, 00887761977853, 00887761977860, 00887761977877, 00887761977884, 00887761977891, 00887761977907, 00887761977914, 00887761977921, 00887761977938, 00887761977945 |
| Serial numbers | 5270, V301BP0007, V301BP0008, V301BP0009, V301BP0010, V301BP0011, V301BP0012, V314BP0013, V314BP0015, V314BP0017, V314BP0018, V314BP0019, V314BP0020, V314BP0021, V314BP0022, V314BP0023, V314BP0024, V314BP0025, V314BP0026, V314BP0027, V314BP0028, V314BP0029, V314BP0030, V314BP0031, V314BP0032 and 475 more |
| Model numbers | 20877002S, 20877003S, 20877004S, 20877007S, 20877008S, 21649301S, 21649401S, 21649402S, P006800A01, P006800A02, P3255A01, P3255A02, P3255A03, P3255ARENT01, P7923A01, P7923A02, P7923A03, P7923A04, P7924A01, P7924A02, P7924A03, P7924A04, P7924ARENT01 |
Product
Hill-Rom pro+ mattress, product codes (REF): a) 20877002S, b) 20877003S, c) 20877004S, d) 20877007S, e) 20877008S, f) 21649301S, g) 21649401S, h) 21649402S, i) P006800A01, j) P006800A02, k) P3255A01, l) P3255A02, m) P3255A03, n) P3255ARENT01, o) P7923A01, p) P7923A02, q) P7923A03, r) P7923A04, s) P7924A01, t) P7924A02, u) P7924A03, v) P7924A04, w) P7924ARENT01
Reason for recall
There is a potential for mattress cover damage (delamination) which may result in fluid absorption in the mattress (fluid ingress).
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-1482-2023. 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.