FDA Adverse Event Summary report: N

MECHANICAL WALKER, ROLLATOR

MDR report key: 2853711 · Received December 3, 2012

Report

Report Number
1531186-2012-01583
Date Received
December 3, 2012
Date of Event
November 1, 2012
Report Date
November 1, 2012
Manufacturer
GENTEEL HOMECARE PRODUCTS
Product Code
ITJ
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TN, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Additional Manufacturer Narrative · 1

THE INCORRECT INFORMATION WAS SUBMITTED ON THE INITIAL MEDWATCH.

Description of Event or Problem · 1

PROVIDER STATES CASTER IS STRIPPED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 MECHANICAL WALKER, ROLLATOR 890.3825 ITJ GENTEEL HOMECARE PRODUCTS UNKNOWN GT080519

Patients

Seq Age Sex Outcome Treatment
1 Other