Invacare Reliant 350 Stand-Up Lift with Power Base RPS350-2Recalls & reported problems
Invacare Corporation · Invacare Reliant 350 Stand-Up Lift with Power Base · 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 00841447103004), received between Nov 21, 2024 and Nov 21, 2024 — 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
- Adverse Event Without Identified Device or Use Problem1
- Insufficient Device Problem Information1
Patient problems
- Bone Fracture(s)1
- Joint Dislocation1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryNov 21, 2024Adverse Event Without Identified Device or Use Problem; Insufficient Device Problem Information; Adverse Event Without Identified Device or Use Problem; Insufficient Device Problem Information
THE PATIENT LIFT WAS INVOLVED IN AN INCIDENT WHERE THE USER WAS JUST HANGING BY THEIR ARMS RESULTING IN A DISLOCATED SHOULDER AND BROKEN HUMERUS. INITIALLY THE FACILITY INDICATED THE USER SHOULD HAVE BEEN USING A DIFFERENT LIFT BUT IN FURTHER CONTACT INDICATED IT WAS THE CORRECT LIFT AND SLING FOR THIS USER. THE LIFT ALLEGEDLY BECAME STUCK IN THE RAISED POSITION FOR ONE MINUTE BEFORE BEGINNING TO LOWER AGAIN. THE USER RECEIVED X-RAYS AT THE HOSPITAL FOLLOWING THE INCIDENT AND WAS INSTRUCTED TO FOLLOW UP WITH AN ORTHOPEDIC SPECIALIST. THE PRODUCT HAS BEEN TAKEN OUT OF USE. THE USER WAS WITHIN THE WEIGHT CAPACITY OF THE DEVICE. TWO CERTIFIED NURSE ASSISTANTS WERE PRESENT DURING THE INCIDENT.
Patient problems: Bone Fracture(s); Joint Dislocation
MAUDE report 20747200 ↗
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- Medline MDS400ELBMedline Industries, Inc. · Lift, patient, non-ac-powered79 reports
- MEDLINE MDS88200HLMedline Industries, Inc. · Lift, patient, non-ac-powered77 reports
- Likorall™ overhead lift 3121001Liko AB · Lift, patient, non-ac-powered1 recall24 reports
- Likorall™ overhead lift 3124050Liko AB · Lift, patient, non-ac-powered1 recall18 reports
- Viking™ XL mobile lift 2040043Liko AB · Lift, patient, non-ac-powered1 recall14 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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