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pro+

HILL-ROM, INC. · Model P7923A08 · UDI-DI 00887761007628

IOQ
10
510(k) clearances
1,202
Adverse events (42 deaths)
38
Recalls
25
Facilities

Description

CENTRELLA® PRO+ 40" SURFACE

Recalls

DateFirmReason
2026-08-18Baxter Healthcare CorporationThere is an error in the product description on the Unique Device Identification (UDI) label. These discrepancies in labeling do not align with the approved product or product spec
2026-08-18Baxter Healthcare CorporationThere is an error in the product description on the Unique Device Identification (UDI) label. These discrepancies in labeling do not align with the approved product or product spec
2026-08-18Baxter Healthcare CorporationThere is an error in the product description on the Unique Device Identification (UDI) label. These discrepancies in labeling do not align with the approved product or product spec
2025-02-25Baxter Healthcare CorporationThe air bladders inside the mattress may move out of position when the head of the bed is elevated, causing a dip in the mattress.
2024-05-08Baxter Healthcare CorporationThere 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 a
2024-03-05Baxter Healthcare CorporationInconsistencies were identified with service records associated with corrections performed for a previous Medical Device Correction issued by Baxter (ref number: FA-2022-026). Your
2023-10-04Baxter Healthcare CorporationProgressa+ beds have the potential for static buildup from the casters and/or power drive. This static electricity could be passed to the operator through the transport handle duri
2023-03-31Baxter Healthcare CorporationThere is a potential for mattress cover damage (delamination) which may result in fluid absorption in the mattress (fluid ingress).
2022-06-24Baxter Healthcare CorporationThe 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 res
2022-06-24Baxter Healthcare CorporationThe 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 res

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.