FDA Adverse Event Malfunction Summary report: N

ENDOPATH** XCEL* TROCAR

MDR report key: 2073076 · Received April 29, 2011

Report

Report Number
3005075853-2011-01800
Event Type
Malfunction
Date Received
April 29, 2011
Date of Event
April 12, 2011
Report Date
April 12, 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
KS
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

(B)(4) AFTER SEVERAL REQUESTS, THE DEVICE WAS NOT RECEIVED FOR ANALYSIS.

Additional Manufacturer Narrative · 1

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

Description of Event or Problem · 1

IT WAS REPORTED THAT DURING AN ENDOSCOPIC THYROIDECTOMY PROCEDURE, THERE WAS AIR LEAKAGE. IT IS UNKNOWN HOW THE PROCEDURE WAS COMPLETED. THERE WERE NO ADVERSE CONSEQUENCES FOR THE PATIENT.

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. NA UNK

Patients

Seq Age Sex Outcome Treatment
1