Invacare Reliant 600 Heavy-Duty Power Lift with Manual Low Base RPL600-1Recalls & reported problems
Invacare Corporation · Invacare Reliant 600 Heavy-Duty Power Lift with Manual Low Base · Class 1
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00841447102977), received between Aug 27, 2025 and Sep 4, 2025 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Break” (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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Break1
- Component Missing1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 4, 2025Component Missing; Component Missing
DEALER STATED THE CUSTOMER IS REQUESTING REPLACEMENT HARDWARE FOR THE SPREADER BAR ON THIS RPL600-1 LIFT. HE SAID THE SPREADER BAR FELL OFF THE OTHER DAY AND SOME OF THE HARDWARE IS NOW MISSING. HE NEEDS THE BOLTS AND SPRINGS FOR THE SPREADER BAR.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22967515 ↗MalfunctionAug 27, 2025Break; Break
THE CONSUMER REPORTED THAT THEY HAVE AN RPL600-1 LIFT AND THE BOLT THAT HOLDS THE HANDLE ON TO THE BASE OF THE LIFT BROKE. THE CONSUMER REQUESTED THE PART NUMBER TO REPLACE THE BOLT. NO OTHER INFORMATION IS AVAILABLE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22906129 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.