FDA Adverse Event Malfunction Summary report: N

5MM PEEK MULTIFUNCTION HANDLE

MDR report key: 4090610 · Received September 15, 2014

Report

Report Number
0002936485-2014-00716
Event Type
Malfunction
Date Received
September 15, 2014
Date of Event
August 25, 2014
Report Date
August 25, 2014
Manufacturer
STRYKER ENDOSCOPY-SAN JOSE
Product Code
KOG
PMA / PMN Number
K973259
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MI, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

ADDITIONAL INFORMATION WILL BE PROVIDED ONCE THE INVESTIGATION HAS BEEN COMPLETED.

Additional Manufacturer Narrative · 1

THE PRODUCT WAS RETURNED AND THE FAILURE MODE WAS CONFIRMED. DURING THE INSPECTION OF THE 5MM PEEK MULTIFUNCTION HANDLE IT WAS CONFIRMED, THE INSULATION IS COMPROMISED. VISIBLE DINGS AND SCRATCHES WERE SEEN THROUGHOUT THE SHAFT. THE 5MM PEEK MULTIFUNCTION HANDLE FAILED THE INSULATION INTEGRITY TEST. IFU 1000401070 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 COULD BE WEAR AND TEAR AND OR MISHANDLING. 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
569940 5MM PEEK MULTIFUNCTION HANDLE ENDOSCOPE AND/OR ACCESSORIES KOG STRYKER ENDOSCOPY-SAN JOSE 1341243H

Patients

Seq Age Sex Outcome Treatment
1