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Leg Support

HILL-ROM, INC. · Model P7625C · UDI-DI 00887761995468

KNC
10
510(k) clearances
602
Adverse events
12
Recalls
6
Facilities

Description

Hospital Bed Accessories

Recalls

DateFirmReason
2025-05-06Baxter Healthcare CorporationThere is a potential for improper crimps on the signal wires of the actuators which could result in a loss of ability to lower the bed or the foot section of the bed.
2021-05-28Hill-Rom, Inc.Latch mechanism on the Lift-Off foot section of the Affinity Four Birthing Bed is damaged, it could potentially cause the installed foot section to be improperly engaged onto the b
2016-07-15Hill-Rom, Inc.
2014-06-26Hill-Rom, Inc.The attachment latch mechanism can become bent depending on user handling. Latch mechanism bending could lead to improper engagement of the foot section and this could result in i
2012-04-02Hill-Rom, Inc.During review of our last braking system via that field corrective action, the system still did not meet our expectations, which is to eliminate the hazards of patient falling. Bed
2007-11-21Hill-Rom, Inc.Hole/opening on the labor bar -- Amputation of a finger could result, if a finger is placed into the opening, as the hole/opening creates a shear point when the mechanism is activa
2007-11-21Hill-Rom, Inc.Hole/opening on the labor bar -- Amputation of a finger could result, if a finger is placed into the opening, as the hole/opening creates a shear point when the mechanism is activa
2007-11-21Hill-Rom, Inc.Hole/opening on the labor bar -- Amputation of a finger could result, if a finger is placed into the opening, as the hole/opening creates a shear point when the mechanism is activa
2007-11-21Hill-Rom, Inc.Hole/opening on the labor bar -- Amputation of a finger could result, if a finger is placed into the opening, as the hole/opening creates a shear point when the mechanism is activa
2006-08-18Hill-Rom, Inc.The cable on the auxiliary outlet may become pinched, which may result in an electrical short with melting of the plastic transformer and the emission of smoke.

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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.