FDA Adverse Event Summary report: N

MECHANICAL WALKER, ROLLATOR

MDR report key: 2981750 · Received February 27, 2013

Report

Report Number
1531186-2013-00785
Date Received
February 27, 2013
Report Date
February 27, 2013
Manufacturer
GENTEEL HOMECARE PRODUCTS
Product Code
ITJ
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

(B)(4). NO SERIOUS INJURY ALLEGED. MALFUNCTION ALLEGED. DEALER STATES WHERE THE CASTER BOLT GOES INTO THE LEG EXTENSION, THE TUBING ISD STRIPPED. MDR FILED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
84280 MECHANICAL WALKER, ROLLATOR 890.3825 ITJ GENTEEL HOMECARE PRODUCTS 68100

Patients

Seq Age Sex Outcome Treatment
1 Other