FDA Device recall Z-1482-2023
Hill-Rom pro+ mattress, product codes (REF): a) 20877002S, b) 20877003S, c) 20877004S, d) 20877007S, e) 20877008S, f) 21649301S, g) 2164940…
- FDA Device
- Class II
- ongoing
- Published 2023-05-10
On 2023-05-10 the FDA classified a Class II recall of Hill-Rom pro+ mattress, product codes (REF): a) 20877002S, b) 20877003S, c) 20877004S, d) 20877007S, e) 20877008S, f) 21649301S, g) 2164940… by Baxter Healthcare, citing there is a potential for mattress cover damage (delamination) which may result in fluid absorption in the mattress (fluid ingress).
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1482-2023 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-03-31 |
| Published | 2023-05-10 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Baxter Healthcare |
| Distribution | US |
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
There is a potential for mattress cover damage (delamination) which may result in fluid absorption in the mattress (fluid ingress).
Identifiers
| code_info | a) 20877002S, UDI/DI N/A, Serial Numbers: W315BP5905, W315BP5907, W315BP5910, W315BP5911; b) 20877003S, UDI/DI N/A,…a) 20877002S, UDI/DI N/A, Serial Numbers: W315BP5905, W315BP5907, W315BP5910, W315BP5911; b) 20877003S, UDI/DI N/A, Serial Numbers: W301BP5612, W301BP5615; c) 20877004S, UDI/DI N/A, Serial Numbers: W231BP4205, W238BP4341, W238BP4342, W238BP4343, W238BP4345, W238BP4347, W238BP4348, W238BP4349, W246BP4519, W246BP4525, W246BP4526, W245BP4502, W245BP4503, W246BP4510, W246BP4511, W246BP4513, W246BP4514, W246BP4520, W246BP4521, W246BP4523, W246BP4524, W252BP4622, W252BP4629, W252BP4634, W252BP4636, W246BP4505, W246BP4512, W252BP4612, W252BP4618, W252BP4620, W256BP4671, W256BP4673, W287BP5300, W287BP5301, W287BP5302, W322BP6072, W322BP6076,; d) 20877007S, UDI/DI N/A, Serial Numbers: W299BP5609, W299BP5611; e) 20877008S, UDI/DI N/A, Serial Numbers: W301BP5616, W301BP5621; f) 21649301S, UDI/DI N/A, Serial Numbers: W188TP7991, W188TP7992, W188TP7993, W188TP7994, W188TP7995, W188TP7996, W188TP7997, W188TP7998; g) 21649401S, UDI/DI N/A, Serial Numbers: W188TP8006, W188TP8007, W1 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1482-2023%22
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