Hill-Rom recalls Progressa Bed model P7500 (serials V133AW9885-V142AW0261) manufactured May 2020 due to potential screw failure causing serious injury during medical use.
Affected beds may have screws installed that do not meet material tensile strength requirements. Failure of this screw could result in serious patient or user injury.
Hill-Rom is recalling Progressa beds with catalog number P7500 that were made between May 12 and May 21, 2020. These beds have screws that may not meet strength requirements, which could cause serious injury to patients or users if the screw fails.
The screws in these beds may not be strong enough to handle normal use. If the screw fails, it could cause serious injury to patients or users, especially during medical treatments that require the bed to be in motion.
Healthcare facilities using Progressa beds for medical therapy, particularly those treating patients with immobility or pressure ulcers. Patients and caregivers at highest risk if the bed is used without proper installation.
Check for Progressa Bed catalog number P7500 with serial numbers starting with V133AW9885 through V142AW0261. These beds were manufactured between May 12 and May 21, 2020.
Look for the serial number on the bed's label to confirm if it falls within the affected range V133AW9885 to V142AW0261.
Reach out to Hill-Rom directly for guidance on next steps if you have an affected bed.
The screws in these beds may not meet material strength requirements, which could lead to serious injury if the screw fails during medical use.
Check your bed's serial number to see if it's affected. If it is, contact Hill-Rom for guidance on next steps.
These beds were manufactured between May 12 and May 21, 2020.
We’ve drafted a message you can send Hill-Rom to request your refund or repair — edit it as you like.
Subject: Recall Z-2737-2020 — Hill-Rom Hill-Rom Hello, I own a Hill-Rom that is covered by recall Z-2737-2020 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.
