Molift Molift Quick Raiser 205 Active FL (Ø50/75mm)Recalls & reported problems
Etac A/S · Class 1
Data updated Oct 18, 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 05707995033185), received between Jul 6, 2026 and Jul 6, 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 18, 2026.
Reports received per month
Most reported problems
Device problems
- Insufficient Device Problem Information1
Patient problems
- Unspecified Skin and Subcutaneous Tissue Problem1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJul 6, 2026Insufficient Device Problem Information
HOVERTECH RECEIVED INFORMATION REGARDING AN INCIDENT IN WHICH AN INDIVIDUAL SUSTAINED A LACERATION TO THE KNEE WHILE BEING TRANSFERRED TO A STANDING POSITION USING THE MOLIFT QUICK RAISER 205. ACCORDING TO THE INFORMATION RECEIVED, THE LIFTING ARM WAS MOVING UPWARD DURING THE TRANSFER WHEN THE INJURY OCCURRED. THE INJURY REQUIRED SEVERAL SUTURES FOR CLOSURE. MOREOVER, IT WAS REPORTED THAT THERE DOES NOT APPEAR TO BE ANY EQUIPMENT FAILURE.
Patient problems: Unspecified Skin and Subcutaneous Tissue Problem
MAUDE report 25725178 ↗
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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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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