FDA Adverse Event Injury Summary report: N

CARDINAL HEALTH ADULT ALUMINUM CRUTCHES

MDR report key: 1697368 · Received May 7, 2010

Report

Report Number
1219232-2010-00001
Event Type
Injury
Date Received
May 7, 2010
Date of Event
March 30, 2010
Report Date
May 6, 2010
Manufacturer
CAREMAX REHABILITATION EQUIP. CO. LTD.
Product Code
IPR
Adverse Event
Yes
Product Problem
Yes
Report Source
Distributor report
Reporter Location
NC, US
Reporter Occupation
NOT APPLICABLE

Narratives

Description of Event or Problem · 1

REPORT OF TALL ADULT CRUTCH BREAKING IN HALF DURING USE RESULTED IN PT INJURY. NUMEROUS ATTEMPTS TO OBTAIN FURTHER INFO REGARDING INCIDENT HAVE BEEN MADE YIELDING NO RESULTS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 CARDINAL HEALTH ADULT ALUMINUM CRUTCHES CRUTCHES IPR CAREMAX REHABILITATION EQUIP. CO. LTD. 75-1435-0001 092324

Patients

Seq Age Sex Outcome Treatment
1 UNK Hospitalization