FDA Adverse Event Other Summary report: N

BIOMET

MDR report key: 210889 · Received January 3, 1999

Report

Report Number
210889
Event Type
Other
Date Received
January 3, 1999
Manufacturer
BIOMET
Product Code
HTT
Adverse Event
Yes
Product Problem
Yes
Report Source
User Facility report
Reporter Occupation
NURSE

Narratives

Description of Event or Problem · 1

DRILL BIT TIMES 2 - BROKEN OFF IN HIP; LEFT IN PT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 BIOMET DRILL BIT HTT BIOMET UNK UNK

Patients

Seq Age Sex Outcome Treatment
1 * Other