PlainRecalls
FDA Devices Moderate Class II Ongoing

Hill-Rom Centrella Pro+ 40" Surface mattress, REF P7923A04.

Reported: July 27, 2022 Initiated: June 24, 2022 #Z-1417-2022

Product Description

Hill-Rom Centrella Pro+ 40" Surface mattress, REF P7923A04.

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.

Details

Units Affected
9 mattresses
Distribution
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.
Location
Deerfield, IL

Frequently Asked Questions

What product was recalled?
Hill-Rom Centrella Pro+ 40" Surface mattress, REF P7923A04.. Recalled by Baxter Healthcare Corporation. Units affected: 9 mattresses.
Why was this product recalled?
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.
Which agency issued this recall?
This recall was issued by the FDA Devices on July 27, 2022. Severity: Moderate. Recall number: Z-1417-2022.