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Baxter Healthcare Corporation recalls Hill-Rom PRO+ 36" MRS Surface mattress, REF P7924A03.
Recalled July 27, 2022 · FDA recall Z-1412-2022 · Baxter Healthcare
Hazard
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. · FDA Class II
Units
404 mattresses
Sold at
Worldwide distribution - US Nationwide distribution in the states of AZ, CA, CO, CT, GA, IA, IN, KY, LA, MD, MI, MN, MO, NC, NJ, NM, NM, NY, OH, OK, RI, SD, TN, TX, VT, and WI. There was government distribution but no military distribution. The country of Canada.
Description
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.
Product
Hill-Rom PRO+ 36" MRS Surface mattress, REF P7924A03.
Manufacturer(s)
Baxter Healthcare Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →