FDA Device recall Z-1413-2022
Hill-Rom PRO+ MRS Surface For Versacare With X-Ray mattress, REF P3255A01
- FDA Device
- Class II
- ongoing
- Published 2022-07-27
On 2022-07-27 the FDA classified a Class II recall of Hill-Rom PRO+ MRS Surface For Versacare With X-Ray mattress, REF P3255A01 by Baxter Healthcare, citing 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 re….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1413-2022 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2022-06-24 |
| Published | 2022-07-27 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Baxter Healthcare |
| Distribution | US |
Product
Hill-Rom PRO+ MRS Surface For Versacare With X-Ray mattress, REF P3255A01.
Reason
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.
Identifiers
| code_info | UDI 00887761977860, Serial numbers: W214BP3955, W214BP3956, W243BP4436, W243BP4438, W243BP4445, W243BP4446, W243BP4447, and W243BP4448. |
|---|
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-1413-2022%22
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