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pro+ P7923A01Recalls & reported problems

Hill-Rom, Inc. · Hospital Bed Surface · Class 2

3 open recalls name this device. See the recall details and contact the manufacturer or your healthcare provider.

Adverse event reports
0
Deaths reported
0
Injuries reported
0
Recalls naming it
3

Summary

No MAUDE adverse event reports in our data reference this device identifier directly.

3 FDA recall records name this device's identifier, 3 still open.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.

Recalls naming this device

  1. May 8, 2024Open, Classified

    There is a potential for the top cover of the hospital bed mattress to delaminate as a result of improper cleaning and lack of adequate details on the appropriate use of cleaning agents containing bleach.

    Z-2151-2024 · Root cause: Error in labeling · FDA record ↗

  2. Mar 31, 2023Open, Classified

    There is a potential for mattress cover damage (delamination) which may result in fluid absorption in the mattress (fluid ingress).

    Z-1482-2023 · Root cause: Process change control · FDA record ↗

  3. Jun 24, 2022Open, Classified

    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.

    Z-1415-2022 · Root cause: Nonconforming Material/Component · FDA record ↗

Other BED, FLOTATION THERAPY, POWERED devices

All BED, FLOTATION THERAPY, POWERED devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.