Baxter Healthcare Corporation: Medical Device Recall in 2022 - (Recall #: Z-1417-2022)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2022.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: June 24, 2022

Date Posted: July 27, 2022

Recall Number: Z-1417-2022

Event ID: 90511

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.

Status: Ongoing

Product Quantity: 9 mattresses

Code Information:

UDI 00887761977914; Serial numbers: W238BP4349, W238BP4350, W238BP4352, W238BP4354, W238BP4355, W238BP4356, W238BP4357, W238BP4358, and W238BP4359.

Distribution Pattern:

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.

Voluntary or Mandated:

Voluntary: Firm initiated