FDA Adverse Event Malfunction Summary report: N

MAESTRO MEDIUM FIXED DURAGUARD

MDR report key: 3946169 · Received July 21, 2014

Report

Report Number
0001811755-2014-02578
Event Type
Malfunction
Date Received
July 21, 2014
Date of Event
June 27, 2014
Report Date
June 27, 2014
Manufacturer
STRYKER INSTRUMENTS-KALAMAZOO
Product Code
HBB
PMA / PMN Number
K041754
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MI, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE REPORTED EVENT OF A BENT FOOT ON THE DURAGUARD WAS CONFIRMED BY A STRYKER SERVICE TECHNICIAN THROUGH VISUAL INSPECTION. BASED ON THE RISK DOCUMENTATION A BENT DURAGUARD CAN OCCUR WHEN EXCESSIVE SIDE LOAD IS APPLIED TO THE FEATURE. DEVICE WAS PLACED IN PARTS RETENTION.

Description of Event or Problem · 1

IT WAS REPORTED DURING SERVICE AT MANUFACTURER FACILITY THAT THE FOOT OF THE DURAGUARD WAS BENT ALLOWING FOR A CONDITION WHERE THE BUR/CUTTING ACCESSORY HAS THE POTENTIAL TO DAMAGE THE BLOOD VESSEL OR MEMBRANE. NO ASSOCIATED PROCEDURE, NO PATIENT INVOLVEMENT, NO DELAY, NO MEDICAL INTERVENTION AND NO ADVERSE CONSEQUENCES WERE REPORTED WITH THIS EVENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
424725 MAESTRO MEDIUM FIXED DURAGUARD MOTOR, DRILL, PNEUMATIC HBB STRYKER INSTRUMENTS-KALAMAZOO 10112

Patients

Seq Age Sex Outcome Treatment
1