FDA Adverse Event Injury Summary report: N

3 POSITION RECLINER DLX-X WIDE BLUE RIDGE 9153641314

MDR report key: 4371259 · Received December 30, 2014

Report

Report Number
1531186-2014-07011
Event Type
Injury
Date Received
December 30, 2014
Report Date
October 30, 2014
Manufacturer
UNKNOWN
Product Code
KMN
Adverse Event
Yes
Product Problem
Yes
Report Source
Distributor report
Reporter Location
AL, US
Reporter Occupation
PATIENT

Narratives

Description of Event or Problem · 1

IT HAS BEEN REPORTED BY AN END USER THAT THE HAND PENDANT ON THE LIFTOUT CHAIR SHE HAS DOES NOT WORK, AND THAT THERE COULD BE A POSSIBLE SHORT IN THE HAND PENDANT. THE CHAIR SOMETIMES GETS STUCK IN THE UP POSITION.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
857345 3 POSITION RECLINER DLX-X WIDE BLUE RIDGE 9153641314 CHAIR AND TABLE, MEDICAL KMN UNKNOWN UNKNOWN

Patients

Seq Age Sex Outcome Treatment
1 Other