FDA Adverse Event Malfunction Summary report: N

MICRO BULLDOG APPLYING FORCEP

MDR report key: 1935408 · Received November 16, 2010

Report

Report Number
1044475-2010-00147
Event Type
Malfunction
Date Received
November 16, 2010
Date of Event
November 1, 2010
Report Date
November 1, 2010
Manufacturer
TELEFLEX MEDICAL
Product Code
DXC
Removal / Correction Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NC, US
Reporter Occupation
NOT APPLICABLE

Narratives

Additional Manufacturer Narrative · 1

THE SAMPLE DEVICE HAS NOT BEEN REC'D, THEREFORE THE INVESTIGATION IS INCOMPLETE AT TIME OF THIS REPORT. A F/U INVESTIGATION REPORT WILL BE SENT WHEN COMPLETED.

Description of Event or Problem · 1

THE EVENT IS REPORTED AS: THE HEAD OF THE DEVICE IS SMALLER THAN THE OLDER DEVICES. THIS DEVICE WON'T HOLD CLIPS PROPERLY. NO PT INJURY REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 MICRO BULLDOG APPLYING FORCEP BULLDOG FORCEP DXC TELEFLEX MEDICAL NA UNK

Patients

Seq Age Sex Outcome Treatment
1