FDA Adverse Event
Malfunction
Summary report: N
HARMONIC ACE 23 CM
MDR report key: 1160699
·
Received September 5, 2008
Report
- Report Number
- 3005075853-2008-01552
- Event Type
- Malfunction
- Date Received
- September 5, 2008
- Date of Event
- August 14, 2008
- Report Date
- August 15, 2008
- 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
- JA
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
INFORMATION IS UNAVAILABLE; DEVICE WAS NOT RETURNED FOR EVALUATION.
Description of Event or Problem · 1
IT WAS REPORTED THAT DURING A GASTRECTOMY PROCEDURE, THE TISSUE PAD WAS PEELED WHEN IT WAS CLEANED. ANOTHER DEVICE WAS USED TO COMPLETE THE CASE. THERE WERE NO ADVERSE CONSEQUENCES TO THE PATIENT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | HARMONIC ACE 23 CM | LFL | ETHICON ENDO-SURGERY, LLC | NA | E4L87K |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | HANDPIECE| GENERATOR |