Progressa® Surface P7520A21Recalls & reported problems
Hill-Rom, Inc. · Hospital Bed Surface · Class 2
1 open recall names 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
- 1
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
1 FDA recall record name this device's identifier, 1 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
- Feb 25, 2025Open, Classified
The air bladders inside the mattress may move out of position when the head of the bed is elevated, causing a dip in the mattress.
Z-1468-2025 · Root cause: Nonconforming Material/Component · FDA record ↗
Other BED, FLOTATION THERAPY, POWERED devices
- Compella™Bariatric Bed P7800AHill-Rom, Inc. · BED, FLOTATION THERAPY, POWERED1 recall1 death362 reports
- pro+ P7924A03Hill-Rom, Inc. · BED, FLOTATION THERAPY, POWERED4 recalls3 reports
- pro+ P7924ARENT01Hill-Rom, Inc. · Bed, Flotation Therapy, Powered3 recalls1 death15 reports
- pro+ P3255A02Hill-Rom, Inc. · BED, FLOTATION THERAPY, POWERED3 recalls8 reports
- pro+ P7924A01Hill-Rom, Inc. · BED, FLOTATION THERAPY, POWERED3 recalls4 reports
- pro+ P3255A01Hill-Rom, Inc. · BED, FLOTATION THERAPY, POWERED3 recalls3 reports
- pro+ P7923A03Hill-Rom, Inc. · BED, FLOTATION THERAPY, POWERED3 recalls2 reports
- pro+ P7923A01Hill-Rom, Inc. · BED, FLOTATION THERAPY, POWERED3 recalls0 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.