FDA Adverse Event Malfunction Summary report: N

CAPTIFLEX¿

MDR report key: 2943349 · Received February 5, 2013

Report

Report Number
3005099803-2013-00712
Event Type
Malfunction
Date Received
February 5, 2013
Date of Event
January 14, 2013
Report Date
January 17, 2013
Manufacturer
BOSTON SCIENTIFIC - COSTA RICA (COYOL)
Product Code
FDI
PMA / PMN Number
K941750
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
GA, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

(B)(4) FOR THE REPORTED EVENT: LOOP FAILED TO RETRACT. THE COMPLAINANT INDICATED THAT THE DEVICE WILL NOT BE RETURNED FOR EVALUATION; THEREFORE, A FAILURE ANALYSIS OF THE COMPLAINT DEVICE COULD NOT BE COMPLETED. IF ANY FURTHER RELEVANT INFORMATION IS IDENTIFIED, A SUPPLEMENTAL MEDWATCH WILL BE FILED.

Description of Event or Problem · 1

IT WAS REPORTED TO BOSTON SCIENTIFIC CORPORATION THAT A CAPTIFLEX SMALL OVAL SNARE WAS USED DURING A COLONOSCOPY PROCEDURE PERFORMED ON (B)(6) 2013. ACCORDING TO THE COMPLAINANT, DURING THE PROCEDURE, THE NURSE EXTENDED THE SNARE LOOP FOR THE PURPOSE OF PERFORMING A POLYPECTOMY INSIDE THE PATIENT'S ASCENDING COLON. WHEN THE NURSE TRIED TO RETRACT THE SNARE, A "GRINDING" WAS FELT AND THE LOOP WOULD NOT RETRACT. THE NURSE TRIED TO RETRACT IT AGAIN, BUT HAD THE SAME ISSUE. THE NURSE DID NOT WANT TO RISK CLOSING THE SNARE BY FORCE AT THE POLYPECTOMY SITE, SO THE SNARE WAS REMOVED FROM THE PATIENT AND FROM SERVICE. THE PROCEDURE WAS COMPLETED USING A SECOND CAPTIFLEX SMALL OVAL SNARE. NO PATIENT COMPLICATIONS WERE REPORTED. THE PATIENT'S CONDITION FOLLOWING THE PROCEDURE WAS REPORTED TO BE FINE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
49408 CAPTIFLEX¿ SMALL OVAL - FLEXIBLE FDI BOSTON SCIENTIFIC - COSTA RICA (COYOL) M00562422 0015513948

Patients

Seq Age Sex Outcome Treatment
1