FDA Adverse Event Malfunction Summary report: N

CUTOM - MEDIUM ATTACH WITH EXT. TAP

MDR report key: 3042437 · Received April 3, 2013

Report

Report Number
1045834-2013-01260
Event Type
Malfunction
Date Received
April 3, 2013
Date of Event
November 1, 2011
Report Date
November 28, 2011
Manufacturer
THE ANSPACH EFFORT, INC.
Product Code
HBC
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
JA
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE DEVICE WAS RECEIVED BY ANSPACH. IF ADDITIONAL INFORMATION IS RECEIVED, A SUPPLEMENTAL REPORT WILL BE SENT.

Description of Event or Problem · 1

THE REPORT RECEIVED FROM (B)(4) STATING THAT THE DEVICE WAS "HEATING, THE COLOR BAND AND BEARING CAME OFF." THE DEVICE WAS NOT BEING USED IN SURGERY. THERE WAS NO REPORTED PT OR USER INJURIES. THERE WAS NO ADDITIONAL INFORMATION PROVIDED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
135876 CUTOM - MEDIUM ATTACH WITH EXT. TAP HBC THE ANSPACH EFFORT, INC.

Patients

Seq Age Sex Outcome Treatment
1