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Invacare Reliant 450 Battery-Powered Lift with Power-Opening Low Base RPL450-2Recalls & reported problems

Invacare Corporation · Invacare Reliant 450 Battery-Powered Lift with Power-Opening Low Base · Class 1

Adverse event reports
2
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00841447102960), received between Jun 5, 2025 and Jul 8, 2025 — classified as 1 injury, 1 malfunction.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (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

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 1 reportsJul 2025: 1 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520261
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Adverse Event Without Identified Device or Use Problem1
  • Detachment of Device or Device Component1
  • Use of Device Problem1

Patient problems

  • Laceration(s)1
  • No Clinical Signs, Symptoms or Conditions1
  • Pneumocephalus1

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • MalfunctionJul 8, 2025Detachment of Device or Device Component; Detachment of Device or Device Component

    WHILE LIFTING A PATIENT FROM THE BED, THE HANGER BAR ON THE RPL450-2 PATIENT LIFT DETACHED FROM THE BOOM. IN THE PROCESS THE BRACKET BECAME BENT, AND THE HANGER BAR FELL ONTO THE CHEST OF THE PATIENT. THE PATIENT FELL ONTO THE BED. NO INJURIES WERE REPORTED OR MEDICAL ATTENTION NEEDED. THIS LIFT IS USED BY MULTIPLE PATIENTS.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 22440051 ↗
  • InjuryJun 5, 2025Use of Device Problem; Adverse Event Without Identified Device or Use Problem; Use of Device Problem; Adverse Event Without Identified Device or Use Problem

    THE REPORTER STATED THE USER WAS IN AN INVACARE PATIENT LIFT AND R114 INVACARE SLING, FOLLOWING THE PROPER CARE PLAN ESTABLISHED BY THE FACILITY. AS THE LIFT WAS BEING TURNED BY A CERTIFIED NURSING ASSISTANT AND ANOTHER CNA WAS NEXT TO THE RESIDENT, THE RESIDENT LEANED TO THE LEFT SIDE AND SLIPPED OUT OF THE SLING. THE RESIDENT FELL TO THE FLOOR AND SUSTAINED LACERATIONS TO THE LEFT FOREHEAD, FOREARM, AND SHIN. THE USER RECEIVED X-RAYS WHICH INDICATED "AIR SPACE AROUND THE BRAIN" (PNEUMOCEPHALUS). THE USER IS FOLLOWING UP WITH THE APPROPRIATE CARE TEAM.

    Patient problems: Laceration(s); Pneumocephalus

    MAUDE report 22150048 ↗

Other LIFT, PATIENT, NON-AC-POWERED devices

All LIFT, PATIENT, NON-AC-POWERED devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.