FDA Adverse Event Injury Summary report: N

2243265-1997-00002

MDR report key: 64841 · Received January 21, 1997

Report

Report Number
2243265-1997-00002
Event Type
Injury
Date Received
January 21, 1997
Date of Event
December 16, 1996
Product Code
KWY
Removal / Correction Number
NA
Report Source
Manufacturer report

Narratives

Description of Event or Problem · 1

ORIGINAL TOTAL HIP ARTHROPLASTY REPORTED AS 12/5/96, IN "DISCRIPTION OF EVENT" BLOCK B5. FOLLOW-UP; WITH UF CONFIRMED ORIGIANL TOTAL HIP ARTHROPLASTY WAS ACTUALLY PERFORMED 12/5/95.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 Implant KWY

Patients

Seq Age Sex Outcome Treatment
1 *