Hill-Rom recalls Centrella Pro+ 36" Surface mattresses with specific serial numbers due to potential increased risk of pressure ulcers from reduced heat/moisture management.
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 Centrella Pro+ 36" Surface mattresses because a defect may reduce their ability to manage heat and moisture, increasing the risk of pressure ulcers for patients. This is a safety issue for medical facilities using these mattresses.
The affected mattresses may not properly pull heat and moisture away from patients, which can lead to increased pressure on skin areas and higher risk of pressure ulcers. This is a medical safety concern for patients in healthcare settings.
Medical facilities that use the recalled Centrella Pro+ 36" Surface mattresses are most at risk, particularly those with patients who need specialized care.
Check for the serial numbers listed in the recall notice: W217BP4016, W217BP4039, W217BP4040, and other specific serial numbers provided in the recall documentation.
Verify if your mattress has one of the listed serial numbers in the recall notice.
The recall is due to a potential reduction in the Microclimate Management feature, which could increase the risk of pressure ulcers for patients.
Check if your mattress has one of the listed serial numbers; if it does, contact Hill-Rom for further instructions.
No, this recall applies only to medical facilities using the mattresses, not home use.
We’ve drafted a message you can send Hill-Rom to request your refund or repair — edit it as you like.
Subject: Recall Z-1416-2022 — Hill-Rom Hill-Rom Hello, I own a Hill-Rom that is covered by recall Z-1416-2022 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.
