Data Foundry

Medical device recalls 2022

Hill-Rom PRO+ 36" MRS Surface With X-Ray mattress — Class II medical device recall Z-1411-2022

Ongoing recall by Baxter Healthcare Corporation, reported 2022-07-27, distributed nationwide. The failure mode on the affected mattresses can cause a reduction in the performance of the Microclimate Manag

Recall numberZ-1411-2022
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmBaxter Healthcare Corporation, Deerfield, IL, United States
Recall initiated2022-06-24
Classified2022-07-20
Reported by FDA2022-07-27
DistributedNationwide (US)
Countries outside the USCA
Quantity200 mattresses
UPC / GTIN / UDI-DI00887761976863, 00887761977907
Serial numbersW218BP4041, W218BP4042, W218BP4043, W218BP4044, W218BP4045, W218BP4046, W218BP4048, W218BP4049, W218BP4050, W218BP4051, W218BP4052, W218BP4053, W218BP4054, W218BP4055, W218BP4056, W218BP4057, W218BP4058, W218BP4059, W218BP4060, W218BP4061, W218BP4062, W218BP4063, W218BP4065, W218BP4066, W218BP4067 and 175 more
Model numbersP7924A01, P7924ARENT01

Product

Hill-Rom PRO+ 36" MRS Surface With X-Ray mattress, REF P7924A01; and REF P7924ARENT01, PRO+ MRS Rental Surface with X-Ray mattress.

Reason for recall

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.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1411-2022. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.