FDA Adverse Event Malfunction Summary report: N

10MM, 33CM RATCHETING HANDLE

MDR report key: 4252376 · Received November 14, 2014

Report

Report Number
0002936485-2014-00930
Event Type
Malfunction
Date Received
November 14, 2014
Date of Event
October 23, 2014
Report Date
October 23, 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 INSPECTION OF THE 10MM, 33CM RATCHETING HANDLE, DINGS AND SCRATCHES WERE NOTICED THROUGHOUT THE SHAFT. ALSO, CRACKS WERE SEEN ON BOTH SIDES OF THE DISTAL TIP OF THE SHAFT. 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
736157 10MM, 33CM RATCHETING HANDLE ENDOSCOPE AND/OR ACCESSORIES KOG STRYKER ENDOSCOPY-SAN JOSE 1042940D

Patients

Seq Age Sex Outcome Treatment
1