FDA Adverse Event Injury Summary report: N

CAREX ROLLING WALKER

MDR report key: 5138864 · Received October 8, 2015

Report

Report Number
2182780-2015-00017
Event Type
Injury
Date Received
October 8, 2015
Date of Event
November 4, 2014
Report Date
October 8, 2015
Manufacturer
R. POON MEDICAL PRODUCTS
Product Code
ITJ
Adverse Event
Yes
Product Problem
Yes
Report Source
Distributor report
Reporter Location
DE, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THIS COMPLAINT WAS JUST RECENTLY DISCOVERED WITHIN THE CORPORATE OFFICE OF CAREX. CAREX WAS PURCHASED BY COMPASS HEALTH BRANDS IN 2014, AND FINAL INTEGRATION OF THE CAREX COMPLAINT MANAGEMENT SYSTEM INTO THE COMPASS HEALTH BRANDS COMPLAINT MANAGEMENT SYSTEM HAS JUST BEEN COMPLETED. DUE TO THE AGE OF THIS COMPLAINT, NO ADDITIONAL INFORMATION IS AVAILABLE AT THIS TIME.

Description of Event or Problem · 1

(B)(6) . CUSTOMER LEANS ON PRODUCT TO REST AND BEAR WEIGHT. CLAIMANT WAS ALLEGEDLY USING ROLLING WALKER WHEN ENTERING A BUILDING IN DE WHEN THE RIGHT SIDE SUPPORT BAR FAILED CAUSING THE CLAIMAINT TO FALL AND FRACTURE HER RIGHT HIP.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
665799 CAREX ROLLING WALKER ROLLATOR ITJ R. POON MEDICAL PRODUCTS FGA22200 0000

Patients

Seq Age Sex Outcome Treatment
1 Other