ULTRACISION HARMONIC ACE
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
(B)(4). WHEN ADDITIONAL INFORMATION IS RECEIVED AND/OR THE DEVICE ANALYSIS HAS BEEN COMPLETED, A SUPPLEMENTAL MEDWATCH WILL BE SENT.
(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.
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 |