FDA Adverse Event Malfunction Summary report: N

SHOULDER PROSTHESIS

MDR report key: 25686 · Received August 14, 1995

Report

Report Number
25686
Event Type
Malfunction
Date Received
August 14, 1995
Date of Event
May 25, 1995
Report Date
July 31, 1995
Manufacturer
HOWMEDICA
Product Code
KWR
Product Problem
Yes
Report Source
User Facility report
Reporter Location
CA, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

BECAME LOOSE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 SHOULDER PROSTHESIS SHOULDER PROSTHESIS KWR HOWMEDICA

Patients

Seq Age Sex Outcome Treatment
1 *