FDA Device recall Z-1416-2022
Hill-Rom Centrella Pro+ 36" Surface mattress, REF P7923A03
- FDA Device
- Class II
- ongoing
- Published 2022-07-27
On 2022-07-27 the FDA classified a Class II recall of Hill-Rom Centrella Pro+ 36" Surface mattress, REF P7923A03 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-1416-2022 |
| 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 Centrella Pro+ 36" Surface mattress, REF P7923A03.
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 00887761977921; Serial numbers: W217BP4016, W217BP4039, W217BP4040, W228BP4177, W228BP4179, W228BP4180, W228BP4189…UDI 00887761977921; Serial numbers: W217BP4016, W217BP4039, W217BP4040, W228BP4177, W228BP4179, W228BP4180, W228BP4189, W228BP4190, W228BP4193, W228BP4194, W228BP4195, W228BP4198, W228BP4199, W228BP4201, W217BP4014, W217BP4015, W217BP4018, W217BP4019, W217BP4024, W217BP4025, W217BP4026, W217BP4027, W217BP4037, W217BP4038, W228BP4173, W228BP4174, W228BP4175, W228BP4185, W228BP4186, W228BP4188, W228BP4196, W228BP4200, W217BP4017, W217BP4020, W217BP4021, W217BP4022, W217BP4023, W217BP4028, W217BP4029, W217BP4030, W217BP4031, W217BP4032, W217BP4033, W217BP4034, W217BP4035, W217BP4036, W228BP4183, W228BP4184, W228BP4191, X012BP7192, X012BP7193, X012BP7194, X012BP7195, X012BP7198, X012BP7199, X012BP7202, X012BP7203, X012BP7204, X012BP7205,X012BP7206, X012BP7207, X012BP7208, X012BP7209, X012BP7210, X012BP7215, X013BP7238, X013BP7239, X013BP7240, X013BP7241, and X013BP7243. |
|---|
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-1416-2022%22
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