FDA Adverse Event Malfunction Summary report: N

CORE IMPACTION DRILL

MDR report key: 2941926 · Received December 21, 2012

Report

Report Number
1811755-2012-04315
Event Type
Malfunction
Date Received
December 21, 2012
Date of Event
November 28, 2012
Report Date
November 30, 2012
Manufacturer
STRYKER INSTRUMENTS KALAMAZOO
Product Code
DZJ
PMA / PMN Number
K040369
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
ID, US
Reporter Occupation
NOT APPLICABLE

Narratives

Additional Manufacturer Narrative · 1

DURING THE DEVICE EVALUATION, CORROSION WAS DISCOVERED WITHIN THE MOTOR, WHICH IS PROBABLE CAUSE OF THE REPORTED BIAS CURRENT ERROR.

Description of Event or Problem · 1

IT WAS REPORTED THAT DURING A SURGICAL PROCEDURE AT THE USER FACILITY, THE DRILL WAS OVERHEATING. BACK-UP EQUIPMENT WAS USED TO COMPLETE THE PROCEDURE. NO DELAY, NO ADVERSE CONSEQUENCES AND NO MEDICAL INTERVENTION WERE REPORTED.

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