Baxter Healthcare Corporation recalls Hill-Rom PRO+ 36" MRS Surface mattresses with serial numbers starting with W225BP or X047BP. The failure may reduce heat/moisture management, increasing pressure ulcer risk for patients.
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.
Baxter Healthcare Corporation is recalling Hill-Rom PRO+ 36" MRS Surface mattresses that could fail to properly manage heat and moisture, raising the risk of pressure ulcers for patients. This is a medical device recall for hospital use.
The mattress may fail to pull heat and moisture away from patients, which can lead to increased pressure ulcer development. This is a medical device that helps prevent skin breakdown in patients with limited mobility.
Healthcare facilities using the affected Hill-Rom mattresses. Patients at risk are those with limited mobility who rely on the mattress for pressure ulcer prevention.
Check for serial numbers starting with W225BP or X047BP as listed in the recall notice. The product is a hospital-grade mattress used in medical facilities.
Verify your mattress serial number against the list of affected numbers provided in the recall notice.
The mattress may fail to properly manage heat and moisture, increasing the risk of pressure ulcers for patients who use it.
Check the serial number against the list of affected numbers starting with W225BP or X047BP provided in the recall notice.
The recall does not specify a remedy, so contact Baxter Healthcare Corporation for further instructions.
We’ve drafted a message you can send Hill-Rom to request your refund or repair — edit it as you like.
Subject: Recall Z-1412-2022 — Hill-Rom Hill-Rom Hello, I own a Hill-Rom that is covered by recall Z-1412-2022 from Hill-Rom. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
