MAUDE Adverse Event Report: ARJOHUNTLEIGH MAGOG INC. MAXI MOVE LIFT; LIFT, PATIENT, AC-POWERED

Device Problem Defective Device (2588)

Patient Problem No Clinical Signs, Symptoms or Conditions (4582)

Event Date 01/27/2022

Event Type  malfunction  

Event Description

Lift worked perfectly to raise patient from the bed.Pressed button to lower patient and it did not work.Attempted this three times.Lift was cut off and restarted again, it did not work.The battery was not low, but it was changed just in case that was the problem.Lift still did not work.The manual pin was removed, and the lever was raised, and the patient was manually lowered to the chair.No injury to the patient noted.Work order for the lift was completed.

• Brand Name: MAXI MOVE LIFT
• Type of Device: LIFT, PATIENT, AC-POWERED
• Manufacturer (Section D): ARJOHUNTLEIGH MAGOG INC.; 2349 w lake st; suite 250; addison IL 60101
• MDR Report Key: 13513680
• MDR Text Key: 285472939
• Report Number: 13513680
• Device Sequence Number: 1
• Product Code: FNG
• Combination Product (y/n): N
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: User Facility
• Reporter Occupation: Other Health Care Professional
• Type of Report: Initial
• Report Date: 02/07/2022

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 02/11/2022
• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Device Operator: Health Professional
• Is the Reporter a Health Professional?: Yes
• Was the Report Sent to FDA?: Yes
• Date Report Sent to FDA: 02/07/2022
• Event Location: Hospital
• Date Report to Manufacturer: 02/11/2022
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: Unknown
• Patient Sequence Number: 1
• Patient Age: 29200 DA
• Patient Sex: Male