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FDA (Device enforcement)Recalled 2022-06-24class ii

Baxter Healthcare Corporation: Hill-Rom Centrella Pro+ 40" Surface mattress, REF P7923A04.

Is my product affected?

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

  • UPC 00887761977914

Check against the official notice below — it lists the full affected range.

What happened

Baxter Healthcare Corporation is recalling Hill-Rom Centrella Pro+ 40" Surface mattresses, model REF P7923A04. The affected mattresses have a failure mode that reduces performance of the Microclimate Management feature, which is designed to pull heat and moisture away from patients. This reduction in performance increases the risk that patients may develop pressure ulcers.

Nine mattresses with specific serial numbers (W238BP4349, W238BP4350, W238BP4352, W238BP4354, W238BP4355, W238BP4356, W238BP4357, W238BP4358, and W238BP4359) have been distributed nationwide across multiple U.S. states, Canada, and to government facilities. The recall record does not specify a remedy or recommended action for affected consumers.

Written by software from the official notice below. Not reviewed by a lawyer.

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.

Details from the source

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. 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. Quantity: 9 mattresses Lot/code info: UDI 00887761977914; Serial numbers: W238BP4349, W238BP4350, W238BP4352, W238BP4354, W238BP4355, W238BP4356, W238BP4357, W238BP4358, and W238BP4359.

Source

Official record: FDA (Device enforcement) ↗

Republished from the official source above; details can change — the source record controls.

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