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LiftMate

The Brewer Company LLC · Model 3000 · UDI-DI 00728564000006

FNG
10
510(k) clearances
1,471
Adverse events (75 deaths)
23
Recalls
57
Facilities

Description

The Brewer LiftMate Patient Lift is used in examination rooms for safely lifting patients with mobility issues onto exam tables.

Recalls

DateFirmReason
2024-01-25Raye's Inc.Retrospective engineering analysis against current ISO standards for hoists has determined: 1. The device cannot physically perform at maximum documented weight specifications when
2022-10-24TollosTwo customers reported four incidents in which the lifting strap broke while lifting a patient. If the IC strap fails during use, the patient may fall causing injury to them or the
2013-01-27Prism Medical Services USAThe firm replaced the recalled carry bar with a plastic insert with a carry bar with a metal insert due to improper installation of the recalled carry bars.
2011-04-01Invacare CorporationComponent Defect. The rear mast connector on certain patient lifts distributed by the firm, may break. Failure of the rear mast connector, while in use would result in a patient b
2009-04-07B.H.M. Medical, Inc.Premature failure of the stitching at the junction of the shoulder strap and sling body of the BHM/Medi-Man Combi Sling used with patient lifts.
2009-01-19Penner Mfg IncIncomplete weld on the pillar mounting bracket
2009-01-19Penner Mfg IncIncomplete weld on the pillar mounting bracket
2009-01-19Penner Mfg IncIncomplete weld on the pillar mounting bracket
2009-01-19Penner Mfg IncIncomplete weld on the pillar mounting bracket
2009-01-19Penner Mfg IncIncomplete weld on the pillar mounting bracket

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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.