FDA Adverse Event Malfunction Summary report: N

OVERHEAD COUNTERPOISE SYSTEM

MDR report key: 96372 · Received June 2, 1997

Report

Report Number
2520313-1997-00023
Event Type
Malfunction
Date Received
June 2, 1997
Date of Event
April 30, 1997
Report Date
June 2, 1997
Manufacturer
HANEL GMBH
Product Code
DXT
Removal / Correction Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CO, US
Reporter Occupation
UNKNOWN

Narratives

Description of Event or Problem · 1

SECTION ON OVERHEAD COUNTERPOISE SYSTEM (OCS) WHICH HOLDS THE HORIZONTAL ARM AND ARM ASSEMBLY (YOKE) FELL, NO SERIOUS INJURY RESULTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 OVERHEAD COUNTERPOISE SYSTEM OVERHEAD COUNTERPOISE SYSTEM DXT HANEL GMBH OCS115 NA

Patients

Seq Age Sex Outcome Treatment
1 UNKNOWN Other