FDA Adverse Event Injury Summary report: N

HOYER 800-556-5438

MDR report key: 348027 · Received August 16, 2001

Report

Report Number
MW1022646
Event Type
Injury
Date Received
August 16, 2001
Date of Event
July 31, 2001
Report Date
August 16, 2001
Manufacturer
HOYER PRODUCTS
Product Code
FSA
Report Source
Voluntary report
Reporter Location
NY, US
Reporter Occupation
NURSE

Narratives

Description of Event or Problem · 1

WHILE TRANSFERRING RESIDENT FROM BED TO CHAIR, THE HOOK ON THE MECHANICAL LIFTER DISENGAGED FROM THE LIFTER PAD AND RESIDENT FELL TO THE FLOOR SUSTAINING AN ABRASION AND HEMATOMA ON LEFT OCCIPITAL AREA WITH SOME BLEEDING NOTED. EXAMINED BY NURSE PRACTITIONER AND TRANSFERRED TO HOSP.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
37514 HOYER 800-556-5438 PATIENT LIFTER SLING FSA HOYER PRODUCTS 0200240 NA

Patients

Seq Age Sex Outcome Treatment
1 80 YR Hospitalization