FDA Adverse Event Malfunction Summary report: N

ULTRACISION CURVED BLADE 32CM

MDR report key: 1203783 · Received October 10, 2008

Report

Report Number
3005075853-2008-02281
Event Type
Malfunction
Date Received
October 10, 2008
Date of Event
September 18, 2008
Report Date
September 18, 2008
Manufacturer
ETHICON ENDO-SURGERY, LLC
Product Code
GEI
PMA / PMN Number
K990362
Removal / Correction Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
IL, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

EVALUATION SUMMARY: THE ANALYSIS SHOWED THAT THE DEVICE WAS RETURNED WITH THE DISTAL TIP OF THE BLADE BROKEN OFF. THE REMAINING BLADE PORTION WAS SCRATCHED. POSSIBLE CAUSES OF BLADE DAMAGE INCLUDING BREAKAGE, ARE EXTERNAL CONTACT DURING PRE-OP OR GENERAL USE, BLADE CONTACT WITH OTHER DEVICES, STAPLES OR CLIPS DURING THE PROCEDURE OR USING ANY MEANS OTHER THAN THE BLADE WRENCH TO ATTACH OR DETACH THE BLADE. ONCE MINOR BLADE DAMAGE HAS OCCURRED, SUBSEQUENT ACTIVATIONS MAY INCREASE DAMAGE SEVERITY AND RESULT IN BLADE "LOCKOUT" LATER IN THE PROCEDURE, AND CONTINUED USAGE CAN RESULT IN A BROKEN BLADE. EACH DEVICE IS VISUALLY INSPECTED AND FUNCTIONALLY TESTED PRIOR TO SHIPMENT, AND DAMAGE OF THIS MAGNITUDE WOULD HAVE BEEN DETECTED AT THIS PROCESS. COMPLAINT INFORMATION IS TRENDED ON A REGULAR BASIS TO DETERMINE IF FURTHER INVESTIGATION IS WARRANTED. THE BATCH HISTORY RECORDS WERE REVIEWED WITH NO ANOMALIES NOTED DURING THE MANUFACTURING PROCESS.

Description of Event or Problem · 1

IT WAS REPORTED THAT DURING A LYSIS OF ADHESIONS AND FULGURATION OF ENDOMETRIOSIS IN AN OPERATIVE LAPAROSCOPY, THE BLADE ON THE DEVICE BROKE. THEY GOT A NEW DEVICE TO COMPLETE THE PROCEDURE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 ULTRACISION CURVED BLADE 32CM GEI ETHICON ENDO-SURGERY, LLC NA E4K769

Patients

Seq Age Sex Outcome Treatment
1 HANDPIECE| GENERATOR