FDA Adverse Event Other Summary report: N

AMBULIFT

MDR report key: 284737 · Received July 5, 2000

Report

Report Number
9617021-2000-00060
Event Type
Other
Date Received
July 5, 2000
Date of Event
April 11, 2000
Report Date
June 27, 2000
Manufacturer
ARJO, LTD.
Product Code
FSA
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Occupation
INVALID DATA

Narratives

Description of Event or Problem · 1

THE FACILITY REPORTED THAT, AFTER REMOVING THE PT FROM THE BATH AND ASSISTING IN DRESSING THE PT, THE CARER MANEUVERED THE PT TO THE SINK WHERE PT COULD STAND. AT THIS POINT, THE HANDLE ON THE HOIST SPUN AROUND VERY QUICKLY, DROPPING THE PT TO THE FLOOR (APPROX. 2 FT.). PT AND CARER WERE UNINJURED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 AMBULIFT PATIENT LIFT FSA ARJO, LTD. ABXXXX NA

Patients

Seq Age Sex Outcome Treatment
1 UNKNOWN Other