FDA Adverse Event Injury Summary report: N

SELF-COMPRESSION PLATE, 12 HOLE, 204MM

MDR report key: 22470 · Received February 14, 1995

Report

Report Number
1123762-1995-09001
Event Type
Injury
Date Received
February 14, 1995
Date of Event
January 12, 1995
Report Date
January 29, 1995
Manufacturer
ZIMMER, INC.
Product Code
HRS
Product Problem
Yes
Report Source
Distributor report
Reporter Location
VA, US
Reporter Occupation
PHYSICIAN

Narratives

Description of Event or Problem · 1

PT HAD BROKEN PLATE AND TWO SCREWS, PLATE AND SCREWS WERE REMOVED AND REPLACED WITH A ZMS INTRAMEDULLARY NAIL.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 SELF-COMPRESSION PLATE, 12 HOLE, 204MM Implant SELF-COMPRESSION PLAE, 12 HOLE, 204MM HRS ZIMMER, INC. NA 59995300

Patients

Seq Age Sex Outcome Treatment
1 74 YR Hospitalization