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Bedside Lift
SIZEWISE RENTALS, L.L.C. · Model LIFTBD · UDI-DI 00845699001033
10
510(k) clearances
1,469
Adverse events (75 deaths)
23
Recalls
58
Facilities
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-01-25 | Raye'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 |
| 2022-10-24 | Tollos | Two 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 |
| 2013-01-27 | Prism Medical Services USA | The 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. |
| 2011-04-01 | Invacare Corporation | Component 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 |
| 2009-04-07 | B.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. |
| 2009-01-19 | Penner Mfg Inc | Incomplete weld on the pillar mounting bracket |
| 2009-01-19 | Penner Mfg Inc | Incomplete weld on the pillar mounting bracket |
| 2009-01-19 | Penner Mfg Inc | Incomplete weld on the pillar mounting bracket |
| 2009-01-19 | Penner Mfg Inc | Incomplete weld on the pillar mounting bracket |
| 2009-01-19 | Penner Mfg Inc | Incomplete weld on the pillar mounting bracket |
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Get your free API keyRead the docsData 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.