FDA Device recall Z-1412-2022
Hill-Rom PRO+ 36" MRS Surface mattress, REF P7924A03
- FDA Device
- Class II
- ongoing
- Published 2022-07-27
On 2022-07-27 the FDA classified a Class II recall of Hill-Rom PRO+ 36" MRS Surface mattress, REF P7924A03 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-1412-2022 |
| 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+ 36" MRS Surface mattress, REF P7924A03.
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 00887761977884; Serial numbers: W225BP4122, W225BP4148, W225BP4154, W225BP4155, W225BP4157, W225BP4158, W225BP4161…UDI 00887761977884; Serial numbers: W225BP4122, W225BP4148, W225BP4154, W225BP4155, W225BP4157, W225BP4158, W225BP4161, W225BP4162, W225BP4167, W225BP4170, W225BP4117, W225BP4124, W225BP4126, W225BP4127, W225BP4129, W225BP4130, W225BP4134, W225BP4138, W225BP4139, W225BP4140, W225BP4141, W225BP4142, W225BP4146, W225BP4152, W225BP4153, W225BP4156, W225BP4159, W225BP4164, W225BP4165, W225BP4166, W225BP4168, W225BP4169, W225BP4171, W225BP4172, W225BP4147, W225BP4118, W225BP4160, W225BP4119, W225BP4120, W225BP4123, W225BP4145, W334BP6515, W337BP6576, W337BP6580, W334BP6516, W337BP6584, W333BP6408, W333BP6410, W334BP6519, W337BP6581, W337BP6582, W337BP6585, W334BP6469, W334BP6485, W334BP6514, W337BP6567, W337BP6568, W337BP6569, W337BP6570, W337BP6571, W337BP6574, W337BP6575, W337BP6577, W337BP6579, W337BP6614, W337BP6615, W337BP6621, W337BP6630, W337BP6636, W337BP6641, W337BP6642, W337BP6643, W337BP6644, W337BP6645, W341BP6675, W341BP6676, W341BP6684, W341BP6646, W341BP6681, W341BP6683, W33 |
|---|
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-1412-2022%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.