FDA Adverse Event Malfunction Summary report: N

4MM DIAMOND BALL

MDR report key: 3140711 · Received May 31, 2013

Report

Report Number
1045834-2013-02243
Event Type
Malfunction
Date Received
May 31, 2013
Date of Event
February 28, 2013
Report Date
February 28, 2013
Manufacturer
DEPUY SNYTHES POWER TOOLS
Product Code
HBC
PMA / PMN Number
K011444
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
JA
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE CUTTER/BURR DEVICE WAS NOT RECEIVED FOR EVALUATION. THEREFORE, THE REPORTED CONDITION WAS NOT CONFIRMED. IF ADDITIONAL INFORMATION IS RECEIVED, A SUPPLEMENTAL REPORT WILL BE SENT. (B)(4).

Description of Event or Problem · 1

REPORT RECEIVED FROM (B)(6) REGARDING A CUTTER/BURR DEVICE IN WHICH THE "STERILE PACK WAS DEFORMED". THE ALLEGED DEFECT WAS OBSERVED UPON RECEIPT OF THE PRODUCT, DURING INSPECTION. THEREFORE, THE DEVICE WAS NOT USED IN SURGERY. NO INJURIES OR MEDICAL INTERVENTION WERE REPORTED. NO ADDITIONAL INFORMATION WAS AVAILABLE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
241903 4MM DIAMOND BALL MOTOR, DRILL, ELECTRIC-CUTTER HBC DEPUY SNYTHES POWER TOOLS F476012160

Patients

Seq Age Sex Outcome Treatment
1