FDA Adverse Event Malfunction Summary report: N

ULTRACISION HARMONIC ACE

MDR report key: 3942312 · Received July 17, 2014

Report

Report Number
3005075853-2014-05059
Event Type
Malfunction
Date Received
July 17, 2014
Date of Event
July 10, 2014
Report Date
July 11, 2014
Manufacturer
ETHICON ENDO-SURGERY, LLC.
Product Code
LFL
PMA / PMN Number
K042777
Removal / Correction Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CH
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

(B)(4). 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). ADDITIONAL INFORMATION. REPROCESSED THE DEVICE WAS RETURNED HORIZONTAL METAL SCRATCHES AT THE BLADE AND WITH THE TISSUE PAD OF THE DEVICE DETACHED. DURING THE VISUAL INSPECTION OF THE INSTRUMENT, IT WAS NOTED THAT THE BLADE HAD EVIDENCE OF HAVING BEEN SCRUBBED WITH A METAL PAD, DAMAGING THE BLADE. IN ADDITION, THE TISSUE PAD OF THE DEVICE WAS DISASSEMBLED. THE DEVICE WAS DISASSEMBLED TO INSPECT THE INTERNAL COMPONENT AND NO ANOMALIES WERE FOUND. DUE TO THE HORIZONTAL METAL SCRATCHES DISCOVERED ON THE INSTRUMENT WHICH IS EVIDENCE OF POSSIBLE REUSE/REPROCESSING, WE ARE UNABLE TO DETERMINE HOW THIS CONDITION IMPACTED THE PERFORMANCE OF THE DEVICE AND THEREFORE CANNOT CONCLUDE ROOT CAUSE. THE EVIDENCE THAT WAS FOUND ON THE INSTRUMENT WAS: TISSUE PAD DETACHED; HORIZONTAL METAL SCRATCHES.

Description of Event or Problem · 1

IT WAS REPORTED THAT DURING AN UNKNOWN PROCEDURE THE WHITE TISSUE PAD FELL OFF. THE FALLEN PIECE DIDN'T FALL INTO THE PATIENT'S BODY. CHANGED TO ANOTHER ONE TO COMPLETE THE PROCEDURE. NO ADVERSE EVENT ON THE PATIENT. ONE DEVICE WILL BE RETURNING.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
419391 ULTRACISION HARMONIC ACE INSTRUMENT, ULTRASONIC SURGICAL LFL ETHICON ENDO-SURGERY, LLC. NA UNK

Patients

Seq Age Sex Outcome Treatment
1 GENERATOR AND HANDPIECE