Bedside Lift LIFTBDRecalls & reported problems
Sizewise Rentals, L.L.C. · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00845699001033), received between Apr 3, 2026 and Apr 3, 2026 — classified as 1 injury.
The most frequently reported specific device problem is “Insufficient Device Problem Information” (1 report).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Device problems
- Insufficient Device Problem Information1
Patient problems
- Bone Fracture(s)1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryApr 3, 2026Insufficient Device Problem Information
THE PATIENT WAS USING A BEDSIDE PATIENT LIFT TO TRANSFER OUT OF BED WHEN THE LIFT MALFUNCTIONED AND/OR BROKE CAUSING THE PATIENT TO FALL TO THE FLOOR AND FRACTURE HIS KNEE. THE TWO LIFTS THAT WERE IN USE BY THE PATIENT ARE (B)(6) (REN107506) WITH MANUFACTURE DATE OF 01-FEB-2021 AND (B)(6) (REN119300) WITH MANUFACTURE DATE OF 08-JUL-2022. BOTH LIFTS WERE THE SAME MODEL AND UDI NUMBER. THIS EVENT OCCURRED ON 16-SEP-2023. THE INITIAL NOTIFICATION RECEIVED ON 20-MAY-2024 INDICATED THAT THE PATIENT EXPERIENCED A FALL AND SUSTAINED A FRACTURED KNEE WHICH DID NOT WARRANT AN MDR AT THAT TIME. A SUBSEQUENT NOTIFICATION RECEIVED ON 05-MARCH-2026 REPORTED THAT THE PATIENT SUSTAINED SERIOUS INJURIES, THEREFORE, MDR SUBMISSION IS NOW WARRANTED.
Patient problems: Bone Fracture(s)
MAUDE report 24783067 ↗
Other Lift, Patient, Ac-Powered devices
- Portable Overhead Lift LIFTOHSizewise Rentals, L.L.C. · Lift, Patient, Ac-Powered1 recall0 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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