FDA Adverse Event Malfunction Summary report: N

5MM, 33CM PEEK MONOPOLAR HANDLE 33CM

MDR report key: 4221688 · Received November 3, 2014

Report

Report Number
0002936485-2014-00873
Event Type
Malfunction
Date Received
November 3, 2014
Date of Event
October 15, 2014
Report Date
October 15, 2014
Manufacturer
STRYKER ENDOSCOPY-SAN JOSE
Product Code
KOG
PMA / PMN Number
K973259
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
DC, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

ADDITIONAL INFORMATION WILL BE PROVIDED ONCE THE INVESTIGATION HAS BEEN COMPLETED. DEVICE EVAL: NOT SPECIFIED.

Additional Manufacturer Narrative · 1

THE PRODUCT WAS RETURNED AND THE FAILURE MODE WAS CONFIRMED. DURING THE INSPECTION OF THE 5MM, 33CM PEEK MONOPOLAR HANDLE 33CM, DINGS AND SCRATCHES WERE NOTICED THROUGHOUT THE SHAFT. THE 5MM, 33CM PEEK MONOPOLAR HANDLE 33CM PASSED THE INSULATION INTEGRITY TEST. HOWEVER, IFU 10000401070 STATES "BEFORE USE, ENSURE THAT THERE ARE NO BREAKS, CHIPS, CRACKS, SCRATCHES, TEARS, OR MISSING/LOOSE COMPONENTS ON THE SHAFT INSULATION, HANDLE, OR HOUSING. DO NOT USE THE INSTRUMENT IF ANY OF THESE DEFECTS ARE PRESENT AS THIS COULD CAUSE UNINTENDED ELECTROSURGICAL BURNS AND LIFE-THREATENING COMPLICATIONS. IF DAMAGE HAS OCCURRED, DISCONTINUE USE AND RETURN THE INSTRUMENT FOR REPAIR OR REPLACEMENT." THE PROBABLE ROOT CAUSE/S COULD BE NORMAL WEAR, USER MISHANDLING OR IMPROPER STERILIZATION. IN SUM, THE PRODUCT WAS RETURNED AND THE FAILURE MODE WAS CONFIRMED.

Description of Event or Problem · 1

IT WAS REPORTED THAT THE INSULATION HAS BEEN COMPROMISED.

Description of Event or Problem · 1

IT WAS REPORTED THAT THE INSULATION HAS BEEN COMPROMISED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
702924 5MM, 33CM PEEK MONOPOLAR HANDLE 33CM ENDOSCOPE AND/OR ACCESSORIES KOG STRYKER ENDOSCOPY-SAN JOSE 1240200D

Patients

Seq Age Sex Outcome Treatment
1