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Baxter Healthcare Corporation recalls Hill-Rom Centrella Pro+ 40" Surface mattress, REF P7923A04.
Recalled July 27, 2022 · FDA recall Z-1417-2022 · 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
9 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 Centrella Pro+ 40" Surface mattress, REF P7923A04.
Manufacturer(s)
Baxter Healthcare Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →