FDA Adverse Event Malfunction Summary report: N

MICRO DRILL MEDIUM STRAIGHT ATTACHMENT

MDR report key: 4213498 · Received October 30, 2014

Report

Report Number
0001811755-2014-03855
Event Type
Malfunction
Date Received
October 30, 2014
Date of Event
October 3, 2014
Report Date
October 3, 2014
Manufacturer
STRYKER INSTRUMENTS-KALAMAZOO
Product Code
EIA
PMA / PMN Number
K032117
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
WA, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THROUGH DISASSEMBLY AND VISUAL INSPECTION IT WAS DETERMINED THE COMPONENTS WERE AFFECTED BY BROKEN DOWN LUBE AND DEBRIS. THE DEVICE LIKELY FAILED FOR HEAT DUE TO BROKEN DOWN LUBE AND DEBRIS AFFECTING THE COMPONENTS INCLUDING THE BEARINGS. BROKEN DOWN LUBE MAY AFFECT THE ROTATIONAL AND DESIGN PROPERTIES OF THE DEVICE CAUSING THE SYMPTOMS. THE DEVICE WAS SCRAPPED AT THE MANUFACTURER.

Description of Event or Problem · 1

IT WAS REPORTED THAT DURING EQUIPMENT TESTING CONDUCTED BY A MANUFACTURER FIELD SERVICE TECHNICIAN AT THE USER FACILITY THE MICRO DRILL MEDIUM STRAIGHT ATTACHMENT WAS OVERHEATING. NO MEDICAL INTERVENTION AND NO ADVERSE CONSEQUENCES WERE REPORTED WITH THIS EVENT. AS THIS EVENT OCCURRED DURING TESTING AT THE USER FACILITY, THERE WAS NO PATIENT INVOLVEMENT AND NO DELAY TO A SURGICAL PROCEDURE.

Description of Event or Problem · 1

IT WAS REPORTED THAT DURING EQUIPMENT TESTING CONDUCTED BY A MANUFACTURER FIELD SERVICE TECHNICIAN AT THE USER FACILITY, THE MICRO DRILL MEDIUM STRAIGHT ATTACHMENT WAS OVERHEATING. NO MEDICAL INTERVENTION AND NO ADVERSE CONSEQUENCES WERE REPORTED WITH THIS EVENT. AS THIS EVENT OCCURRED DURING TESTING AT THE USER FACILITY, THERE WAS NO PATIENT INVOLVEMENT AND NO DELAY TO A SURGICAL PROCEDURE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
694911 MICRO DRILL MEDIUM STRAIGHT ATTACHMENT DENTAL OPERATIVE UNIT AND ACCESSORIES. EIA STRYKER INSTRUMENTS-KALAMAZOO 11109

Patients

Seq Age Sex Outcome Treatment
1