FDA Adverse Event
Injury
Summary report: N
PREMIUM SURGICLIP S-9.0 TITANIUM
MDR report key: 3609017
·
Received January 27, 2014
Report
- Report Number
- 2647580-2014-00053
- Event Type
- Injury
- Date Received
- January 27, 2014
- Report Date
- January 7, 2014
- Manufacturer
- COVIDIEN, FORMERLY USSC PUERTO RICO
- Product Code
- FZP
- PMA / PMN Number
- K853650
- Adverse Event
- Yes
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- TX, US
- Reporter Occupation
- PHYSICIAN
Narratives
Additional Manufacturer Narrative · 1
(B)(4).
Description of Event or Problem · 1
ACCORDING TO THE REPORTER: THE SURGEON DESCRIBED OVERALL EXPERIENCE USING THE 134046 OPEN CLIP APPLIER DURING PROCEDURES THAT INCLUDED THE CLIP APPLIER MISFIRING WHICH RESULTED IN CUTTING VESSELS, CLIP MALFORMATIONS/SCISSORING AND UNIT JAMMING BEFORE ALL CLIPS HAD FIRED. HE STATED THAT ADDITIONAL UNITS HAD TO BE USED TO REPLACE THE MALFUNCTIONED ONES AS WELL AS 15-20 MINUTES OF ADDITIONAL PROCEDURE TIME FOR VESSEL REPAIRS AND TROUBLESHOOTING. SPECIFIC DATES, PROCEDURES AND PATIENTS WERE NOT PROVIDED AT THE DISCUSSION.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 58364 | PREMIUM SURGICLIP S-9.0 TITANIUM | DISPOSABLE CLIP APPLIER | FZP | COVIDIEN, FORMERLY USSC PUERTO RICO |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Other |