FDA Device recall Z-1414-2022
Hill-Rom PRO+ MRS Surface For Versacare mattress, REF P3255A02
- 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 mattress, REF P3255A02 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-1414-2022 |
| 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 mattress, REF P3255A02.
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 00887761977853; Serial numbers: W236BP4315, W236BP4320, W236BP4326, W235BP4284, W235BP4294, W236BP4318, W236BP4319,…UDI 00887761977853; Serial numbers: W236BP4315, W236BP4320, W236BP4326, W235BP4284, W235BP4294, W236BP4318, W236BP4319, W236BP4323, W236BP4325, W236BP4331, W236BP4333, W236BP4334, W236BP4336, W235BP4270, W235BP4271, W235BP4272, W235BP4278, W235BP4279, W235BP4287, W235BP4291, W235BP4292, W235BP4299, W235BP4307, W235BP4311, W236BP4314, W236BP4321, W236BP4322, W236BP4324, W236BP4329, W236BP4335, W235BP4309, W235BP4313, W215BP3994, W215BP3995, W215BP4002, W215BP4009, W215BP4011, W214BP3979, W214BP3980, W214BP3981, W214BP3982, W214BP3983, W215BP3985, W215BP3986, W215BP3990, W215BP3992, W215BP3993, W215BP3984, W215BP3987, W215BP3988, W215BP3989, W215BP3991, W215BP3996, W215BP4001, W215BP4003, W215BP4005, W215BP4006, W235BP4282, W235BP4285, W235BP4286, W235BP4289, W235BP4293, W235BP4295, W235BP4298, W235BP4300, W235BP4301, W235BP4302, W235BP4303, W235BP4304, W235BP4305, W235BP4306, W235BP4308, W236BP4316, W236BP4317, W236BP4327, W236BP4328, W236BP4330, W236BP4337, W214BP3968, W214BP3969, W214 |
|---|
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-1414-2022%22
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