FDA Adverse Event Malfunction Summary report: N

ENDOSTAT 3 BIPOLAR/MONOPOLAR ELECTROSURGICAL GENERATOR

MDR report key: 2973864 · Received February 22, 2013

Report

Report Number
3005099803-2013-01041
Event Type
Malfunction
Date Received
February 22, 2013
Date of Event
February 4, 2013
Report Date
February 5, 2013
Manufacturer
BOSTON SCIENTIFIC - MARLBOROUGH
Product Code
KNS
PMA / PMN Number
K913881
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
GA, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

EXACT PATIENT AGE IS UNKNOWN BUT IS OVER 18 YEARS. (B)(4). THE DEVICE HAS NOT BEEN RECEIVED FOR ANALYSIS. UPON RECEIPT AND COMPLETION OF THE FAILURE ANALYSIS OF THE COMPLAINT DEVICE, IF THERE IS ANY FURTHER RELEVANT INFORMATION FROM THAT REVIEW, A SUPPLEMENTAL MEDWATCH WILL BE FILED.

Additional Manufacturer Narrative · 1

INVESTIGATION RESULTS VISUAL EVALUATION OF THE COMPLAINT DEVICE FOUND THE UNIT TO BE IN GOOD CONDITION. ALL THE KNOBS AND SWITCHES APPEAR TO FUNCTION PROPERLY AND THE UNIT PASSED THE ENDOSTAT III RETURN EVALUATION PROCEDURE AND WAS WITHIN ALL TEST PARAMETERS. THE CONDITION OF THE RETURNED DEVICE WAS NOT CONSISTENT WITH THE COMPLAINT; THE COMPLAINT WAS NOT CONFIRMED. THE UNIT PASSED THE ENDOSTAT III RETURN EVALUATION PROCEDURE AND IS WITHIN ALL TEST PARAMETERS. ALL CONNECTIONS INSIDE THE UNIT WERE CHECKED AND WIRES WERE MANIPULATED WHILE THE RF WAS ACTIVATED IN ALL MODES AND NO PROBLEMS COULD BE FOUND WITH THE OUTPUT. A REVIEW OF THE DEVICE HISTORY RECORD (DHR) WAS PERFORMED AND CONFIRMED THAT THIS DEVICE MET ALL MATERIAL, ASSEMBLY AND PERFORMANCE SPECIFICATIONS.

Description of Event or Problem · 1

IT WAS REPORTED TO BOSTON SCIENTIFIC CORPORATION THAT AN ENDOSTAT III ELECTROSURGICAL UNIT WAS USED DURING AN ESOPHAGOGASTRODUODENOSCOPY (EGD) HEMOSTASIS PROCEDURE PERFORMED ON (B)(6) 2013. ACCORDING TO THE COMPLAINANT, DURING THE PROCEDURE, THE DEVICE POWERED UP NORMALLY AND NO ABNORMAL SOUNDS WERE NOTED; HOWEVER, THE UNIT FAILED TO DELIVER ENERGY. THE GOLD PROBE WAS REPLACED, BUT THE SAME ISSUE WAS OBSERVED. THE PROCEDURE WAS COMPETED USING A SECOND ENDOSTAT III ELECTROSURGICAL UNIT. THE DEVICE HAS BEEN TESTED SINCE THIS INCIDENT AND IS VERY SLOW TO DELIVER ENERGY IN MONOPOLAR AND BIPOLAR MODES. THERE WERE NO PATIENT COMPLICATIONS REPORTED AS A RESULT OF THIS EVENT. THE PATIENT'S CONDITION FOLLOWING THE PROCEDURE WAS REPORTED TO BE "GOOD."

Description of Event or Problem · 1

IT WAS REPORTED TO BOSTON SCIENTIFIC CORPORATION THAT AN ENDOSTAT III ELECTROSURGICAL UNIT WAS USED DURING AN ESOPHAGOGASTRODUODENOSCOPY (EGD) HEMOSTASIS PROCEDURE PERFORMED ON (B)(6) 2013. ACCORDING TO THE COMPLAINANT, DURING THE PROCEDURE, THE DEVICE POWERED UP NORMALLY AND NO ABNORMAL SOUNDS WERE NOTED; HOWEVER, THE UNIT FAILED TO DELIVER ENERGY. THE GOLD PROBE WAS REPLACED, BUT THE SAME ISSUE WAS OBSERVED. THE PROCEDURE WAS COMPETED USING A SECOND ENDOSTAT III ELECTROSURGICAL UNIT. THE DEVICE HAS BEEN TESTED SINCE THIS INCIDENT AND IS VERY SLOW TO DELIVER ENERGY IN MONOPOLAR AND BIPOLAR MODES. THERE WERE NO PATIENT COMPLICATIONS REPORTED AS A RESULT OF THIS EVENT. THE PATIENT'S CONDITION FOLLOWING THE PROCEDURE WAS REPORTED TO BE "GOOD."

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
78574 ENDOSTAT 3 BIPOLAR/MONOPOLAR ELECTROSURGICAL GENERATOR UNIT, ELECTROSURGICAL, ENDOSCOPIC (WITH OR WITHOUT ACCESSORIES) KNS BOSTON SCIENTIFIC - MARLBOROUGH M00540200

Patients

Seq Age Sex Outcome Treatment
1