MAUDE Adverse Event Report: INVAMEX RELIANT POWER LIFT W/LOW BASE-PLUS; LIFT, PATIENT, NON-AC-POWERED

Model Number	RPL450-1
Medical Device Problem Code	Detachment of Device or Device Component (2907)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
There was no patient involvement or injury alleged with this incident.The alleged issue with the rpl450-1 patient transport lift hanger bar hardware could not be confirmed and the underlying cause has not been determined.The description of the alleged issue is consistent with a previously investigated issue.This lift was manufactured by invacare invamex november 2011 which is prior to design changes, updates to work instructions and user instructions clarifying maintenance and replacement instructions.The lift is past its end of life of 8 years.If additional information is received, a follow-up report will be filed.
Event or Problem Description
The dealer reported that the pin that attaches the hanger bar on the rpl450-1 patient lift keeps coming out on the lift.

• Brand Name: RELIANT POWER LIFT W/LOW BASE-PLUS
• Common Device Name: LIFT, PATIENT, NON-AC-POWERED
• Manufacturer (Section D): INVAMEX; avenida el puente s/n; parque industrial el puente ma; reynosa, tamaulipas 88783 ; MX 88783
• Manufacturer (Section G): INVAMEX; avenida el puente s/n; parque industrial el puente ma; reynosa, tamaulipas 88783 ; MX 88783
• Manufacturer Contact: dona bhamra ; one invacare way; elyria, OH 44035 ; 8003336900
• MDR Report Key: 24189790
• Report Number: 9616091-2026-00001
• Device Sequence Number: 18175648
• Product Code: FSA
• UDI-Device Identifier: 00841447102953
• UDI-Public: 00841447102953
• Combination Product (Y/N): Y
• Initial Reporter State: MO
• Initial Reporter Country: US
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Other
• Initial Reporter Occupation: Non-Healthcare Professional
• Type of Report: Initial
• Report Date (Section B): 01/27/2026

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Operator of Device: Other
• Device Model Number: RPL450-1
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 12/30/2025
• Initial Report FDA Received Date: 01/27/2026
• Was Device Evaluated by Manufacturer? (Y/N): No
• Date Device Manufactured: 10/01/2011
• Is the Device Labeled for Single Use? (Y/N): No
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Reuse
• Patient Sequence Number: 1
• Patient Sex: Unknown