FDA Adverse Event Injury Summary report: N

ARTHREX PUSHLOCK 4.5 MM X 18.5 MM

MDR report key: 1060697 · Received June 10, 2008

Report

Report Number
MW5007305
Event Type
Injury
Date Received
June 10, 2008
Date of Event
June 9, 2008
Report Date
June 10, 2008
Manufacturer
ARTHREX, INC.
Product Code
HWC
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
MO, US
Reporter Occupation
RISK MANAGER

Narratives

Description of Event or Problem · 1

AFTER PUSH LOCK TAPPED INTO BONE, EYELET OF ANCHOR BROKE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 ARTHREX PUSHLOCK 4.5 MM X 18.5 MM PUSHLOCK 4.5 MM X 18.5 MM HWC ARTHREX, INC. AR-1922 PS

Patients

Seq Age Sex Outcome Treatment
1 Disability