FDA Adverse Event Malfunction Summary report: N

KEYLESS CHUCK/TRINKLE

MDR report key: 149053 · Received February 12, 1998

Report

Report Number
2219689-1998-00099
Event Type
Malfunction
Date Received
February 12, 1998
Report Date
February 11, 1998
Manufacturer
SURGIQUIP INC
Product Code
HTW
Product Problem
Yes
Report Source
Distributor report
Reporter Location
NE, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

THE KEYLESS CHUCK WOULD NOT FIT THE DRILL. THE EVENT DID NOT OCCUR DURING A SURGICAL PROCEDURE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 KEYLESS CHUCK/TRINKLE INSTRUMENT HTW SURGIQUIP INC NA AHC121A

Patients

Seq Age Sex Outcome Treatment
1 NA Other