FDA Adverse Event Malfunction Summary report: N

V. MUELLER

MDR report key: 81122 · Received April 2, 1997

Report

Report Number
MW1010811
Event Type
Malfunction
Date Received
April 2, 1997
Date of Event
February 19, 1997
Report Date
March 10, 1997
Manufacturer
V-MUELLER BAXTER HEALTHCARE
Product Code
GEG
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
CO, US
Reporter Occupation
INVALID DATA

Narratives

Description of Event or Problem · 1

AT THE COMPLETION OF THE CASE, SURGEON NOTICED THAT A SMALL PIECE OF THE ELEVATOR FREER WAS MISSING. IT IS UNKNOWN WHETHER IT WAS RETAINED IN THE PT OR LOST ELSEWHERE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 V. MUELLER ELEVATOR FREER GEG V-MUELLER BAXTER HEALTHCARE RH-750 *

Patients

Seq Age Sex Outcome Treatment
1 53 YR Other