Bed, Flotation Therapy, Powered
Hill-rom, Inc.'s record for this product code
Recent MDR events
321 adverse event reports on file
- PRO+Jun 17, 2026Malfunction25531774
- PRO+Sep 16, 2025Malfunction23062722
- PRO+Aug 18, 2025Malfunction22827097
- PRO+Aug 15, 2025Malfunction22814477
- HILLROM CENTRELLA BEDMay 7, 2025InjuryMW5170053
- HILLROM MATTRESS TOP COVERMar 26, 2025MalfunctionMW5168288
- BED, FLOTATION THERAPY, POWEREDFeb 5, 2025InjuryMW5165666
- BED, FLOTATION THERAPY, POWEREDFeb 5, 2025MalfunctionMW5165667
- 882Nov 29, 2024InjuryMW5163019
- VERSACARE P500Nov 21, 2024MalfunctionMW5162879
Recalls
2 recall events for this product code
- TerminatedJul 23, 2013
When the bed is put into the chair egress position, the magnets on the mattress may not hold the bottom of the mattress flat to the bed frame, and the mattress foot section will extend away from the bed at an angle. A patient attempting to get back into the bed may miss the seat and sit on the foot section instead. The patient can slide down to the floor, or fall, with possible injury.
View FDA record ↗ - TerminatedMar 14, 2013
In certain situations a software problem with the TotalCare SpO2RT 2 bed may occur that can lead to inadvertent loss of sufficient surface cushion pressure to adequately support the patient. This may increase the likelihood of skin irritation for patients at higher risk of developing pressure-related skin conditions. A correction to the software program is currently being developed and tested,
View FDA record ↗
510(k) clearances
5 clearances for this product code