FDA Adverse Event Malfunction Summary report: N

ENDOPATH** XCEL* TROCAR

MDR report key: 2071471 · Received April 28, 2011

Report

Report Number
3005075853-2011-01762
Event Type
Malfunction
Date Received
April 28, 2011
Date of Event
April 8, 2011
Report Date
April 11, 2011
Manufacturer
ETHICON ENDO-SURGERY, LLC.
Product Code
GCJ
PMA / PMN Number
K032676
Removal / Correction Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
AL, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

(B)(4). THE ANALYSIS RESULTS FOUND THAT THE DEVICE WAS RETURNED IN GOOD CONDITION. IN AN ATTEMPT TO REPLICATE THE REPORTED INCIDENT, THE DEVICE WAS FUNCTIONALLY TESTED TO DETECT ANY LEAKING ISSUES. UPON EVALUATION OF THE DEVICE, IT WAS FUNCTIONALLY LEAK TESTED AND PASSED. THE DEVICE WAS FULLY FUNCTIONAL ACCORDING TO THE MANUFACTURING REQUIREMENTS. NO CONCLUSION COULD BE REACHED AS TO WHAT MAY HAVE CAUSED THE REPORTED INCIDENT. AS THE OBTURATOR WAS NOT RECEIVED AND IT IS THE PART THAT HAS THE BATCH STAMPED, WE DID NOT RECEIVE A BATCH OR LOT NUMBER FOR THE PRODUCT INVOLVED IN THIS COMPLAINT. THEREFORE, WE WERE UNABLE TO CHECK MANUFACTURING RECORDS FOR ANY RELATED NON-CONFORMANCES.

Additional Manufacturer Narrative · 1

(B)(4). INFORMATION ANTICIPATED, BUT UNAVAILABLE AT THIS TIME.

Description of Event or Problem · 1

IT WAS REPORTED THAT DURING A LAPAROSCOPIC LOW ANTERIOR RESECTION PROCEDURE, THERE WAS CONTINUOUS PNEUMO LEAKAGE THE ENTIRE CASE. THEY EXPERIENCED BLOW BACK OF BLOOD ONTO THE ABDOMEN AS WELL AS THE TOP OF THE TROCAR DUE TO THE LEAKAGE. THERE WAS NO TORQUE OR TWISTING OBSERVED BY THE SALES REP. THE TROCAR WAS USED TO COMPLETE THE PROCEDURE. NO IMPACT TO THE PATIENT REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 ENDOPATH** XCEL* TROCAR LAPAROSCOPE, GENERAL AND PLASTIC SURGERY GCJ ETHICON ENDO-SURGERY, LLC. UNK UNK

Patients

Seq Age Sex Outcome Treatment
1