Hill-Rom recalls specific PRO+ 36" MRS X-Ray mattresses due to potential failure in Microclimate Management feature, increasing patient risk of pressure ulcers. Affected units have listed serial numbers.
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.
Hill-Rom is recalling certain PRO+ 36" MRS X-Ray mattresses because a failure in the Microclimate Management feature could lead to increased patient risk of pressure ulcers. This recall affects specific models with listed serial numbers.
The affected mattresses may fail to properly manage heat and moisture, which can increase the risk of pressure ulcers in patients. This happens because the Microclimate Management feature is designed to pull moisture away from the patient, and its failure could lead to skin breakdown.
Healthcare facilities using the recalled mattresses are most at risk, particularly those with patients who require pressure ulcer prevention.
Check for serial numbers listed in the recall notice: W218BP4042, W218BP4054, and other specific numbers provided in the recall document. The product is a Hill-Rom PRO+ 36" MRS Surface With X-Ray mattress.
Verify if your mattress has a serial number from the list provided in the recall notice.
The recall is due to a potential failure in the Microclimate Management feature that could increase patient risk of pressure ulcers.
The affected models are Hill-Rom PRO+ 36" MRS Surface With X-Ray mattress with serial numbers listed in the recall notice.
No, the recall does not require immediate discontinuation; affected units should be checked against the list.
We’ve drafted a message you can send Hill-Rom to request your refund or repair — edit it as you like.
Subject: Recall Z-1411-2022 — Hill-Rom Hill-Rom Hello, I own a Hill-Rom that is covered by recall Z-1411-2022 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
