FDA Adverse Event Malfunction Summary report: N

CORE IMPACTION DRILL

MDR report key: 2200946 · Received July 1, 2011

Report

Report Number
1811755-2011-02382
Event Type
Malfunction
Date Received
July 1, 2011
Date of Event
June 6, 2011
Report Date
June 8, 2011
Manufacturer
STRYKER INSTRUMENTS KALAMAZOO
Product Code
DZJ
PMA / PMN Number
K040369
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MO, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

THE DRIVESHAFT AND ROTOR WERE STUCK TOGETHER DUE TO CORROSION. ROTOR RUB WAS IDENTIFIED AS THE PROBABLE CAUSE OF THE OVERHEATING.

Description of Event or Problem · 1

THE CORE IMPACTION DRILL WAS SENT IN FOR EVALUATION DUE TO OVERHEATING DURING A TOOTH EXTRACTION PROCEDURE. THE PROCEDURE WAS COMPLETED WITH A READILY AVAILABLE REPLACEMENT DEVICE WITHOUT ANY PROCEDURE DELAY. NO ADVERSE EVENT WAS ASSOCIATED WITH THE DEVICE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 CORE IMPACTION DRILL DZJ STRYKER INSTRUMENTS KALAMAZOO

Patients

Seq Age Sex Outcome Treatment
1 UNK