FDA Adverse Event Malfunction Summary report: N

ENSEAL SUPER JAW

MDR report key: 2366140 · Received December 12, 2011

Report

Report Number
3005075853-2011-05368
Event Type
Malfunction
Date Received
December 12, 2011
Date of Event
November 22, 2011
Report Date
November 22, 2011
Manufacturer
ETHICON ENDO-SURGERY, LLC.
Product Code
GEI
Removal / Correction Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
IN, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

(B)(4). INFORMATION NOT ASKED FOR BUT UNKNOWN OR PROVIDED DURING INITIAL CONTACT. INFORMATION ANTICIPATED, BUT UNAVAILABLE AT THIS TIME. WHEN ADDITIONAL INFORMATION IS RECEIVED AND/OR THE DEVICE ANALYSIS HAS BEEN COMPLETED, A SUPPLEMENTAL MEDWATCH WILL BE SENT.

Additional Manufacturer Narrative · 1

(B)(4). THE DEVICE WAS RECEIVED IN GOOD CONDITION. THE DEVICE WAS TESTED ON THE GENERATOR AND PASSED ALL FUNCTIONAL TESTING. THE ENERGY OUTPUT DELIVERED FROM THE DEVICE WAS VERIFIED AND THE CUTTING OF THE TEST MEDIA PERFORMED AS EXPECTED. ALL THREE TONES WERE HEARD DURING FUNCTIONAL TESTING (TONE 1 IS HEARD WHEN THE ENERGY ACTIVATION BUTTON IS PRESSED; TONE 2 IS HEARD WHEN TISSUE IMPEDANCE THRESHOLD IS REACHED; AND TONE 3 IS HEARD WHEN THE CYCLE IS COMPLETE). DURING FUNCTIONAL TESTING, THE BLADE DID NOT RETURN AFTER THE HANDLE WAS DEPRESSED AND THE JAW DID NOT OPEN. THE JAWS WERE OPENED BY APPLYING AN OPENING FORCE ON THE HANDLE WITH TWO HANDS. THE KNIFE BLADE WAS BUCKLED WHICH RESULTED IN THE JAWS NOT OPENING.

Description of Event or Problem · 1

IT WAS REPORTED THAT DURING A TOTAL ABDOMINAL HYSTERECTOMY PROCEDURE, THE BLADE BENT WHILE GOING THROUGH TISSUE. THE DEVICE WAS HARD TO SQUEEZE AND THE DEVICE WOULD NOT OPEN. ANOTHER DEVICE WAS USED TO COMPLETE THE PROCEDURE. THERE WERE NO ADVERSE CONSEQUENCES FOR THE PATIENT. DID THE SURGEON ATTEMPT TO MANUALLY OPEN THE JAWS WITH HIS FINGERS? YES.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 ENSEAL SUPER JAW ENSEAL SUPER JAW GEI ETHICON ENDO-SURGERY, LLC. UNK H44826

Patients

Seq Age Sex Outcome Treatment
1 GENERATOR AND HANDPIECE