FDA Adverse Event Malfunction Summary report: N

CORE MICRO DRILL

MDR report key: 2140450 · Received June 17, 2011

Report

Report Number
1811755-2011-02232
Event Type
Malfunction
Date Received
June 17, 2011
Date of Event
May 24, 2011
Report Date
May 25, 2011
Manufacturer
STRYKER INSTRUMENTS KALAMAZOO
Product Code
HBE
PMA / PMN Number
K032303
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

CORROSION DAMAGE WAS NOTED WITHIN THE INTERNAL COMPONENTS OF THE DEVICE.

Description of Event or Problem · 1

THE CORE MICRO DRILL WAS SENT IN FOR EVAL DUE TO OVERHEATING. THERE WAS NO PT INVOLVEMENT; NO ADVERSE EVENT WAS ASSOCIATED WITH THE DEVICE.

Devices

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

Patients

Seq Age Sex Outcome Treatment
1 UNK