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Lift, Patient, Ac-Powered

FDA product code FNG · Class 2 · General Hospital

87
Registered devices
1,469
Adverse events
23
Recalls
21
510(k) clearances

Devices with this code

Recent 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
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 i
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 r
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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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.