PROXIMATE** LINEAR STAPLER
Report
- Report Number
- 3005075853-2014-04477
- Event Type
- Malfunction
- Date Received
- June 27, 2014
- Date of Event
- May 28, 2014
- Report Date
- May 28, 2014
- Manufacturer
- ETHICON ENDO-SURGERY, LLC.
- Product Code
- GDW
- PMA / PMN Number
- K020779
- Removal / Correction Number
- NA
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- SN
- Reporter Occupation
- OTHER
Narratives
(B)(4) - LOCKOUT SLIDE TIP DAMAGED, DAMAGED ADJUSTING KNOB. THE ANALYSIS RESULTS SHOWED THAT THE TLH60 DEVICE WAS RECEIVED IN GOOD VISUAL CONDITIONS AND WITH CARTRIDGE PRESENT ON THE DEVICE. THE DEVICE WAS TESTED FOR FUNCTIONALITY WITH A TEST CARTRIDGE AND IT FORMS THE STAPLES AS INTENDED AND WITH A PROPER B FORMATION. THE DEVICE WAS DISASSEMBLED TO VERIFY THE CONDITION OF THE INTERNAL COMPONENTS AND THE DEVICE WAS NOTED TO HAVE THE LOCKOUT TAB AND THE ADJUSTING KNOB DAMAGED. THE DAMAGE TO THE TAB AND KNOB IS CONSISTENT WITH AN EXCESSIVE FORCE APPLIED TO THE ROTATING KNOB WHEN TRYING TO DIAL DOWN A LOCKED DEVICE, CAUSING THE DAMAGE TO THE KNOB. IT SHOULD BE NOTED THAT THE INSTRUMENT HAS BEEN DESIGNED WITH A LOCKOUT FEATURE, WHICH DURING THE FIRST APPLICATION, PREVENTS TURNING THE ADJUSTING KNOB UNLESS THE RETAINING PIN IS PUSHED COMPLETELY FORWARD. PLEASE REFERENCE THE INSTRUCTIONS FOR USE FOR ADDITIONAL INFORMATION. A BATCH RECORD REVIEW WAS PERFORMED AND THE BATCH HAD NO ANOMALIES NOTED DURING THE MANUFACTURING PROCESS.
IT WAS REPORTED THAT DURING AN UNKNOWN PROCEDURE, THE ROTATION KNOB COULDN'T ROTATE; HENCE SURGEON COULDN'T COMPRESS THE TISSUE. PROCEDURE WAS COMPLETED WITH SAME LIKE DEVICE. NO PATIENT CONSEQUENCES REPORTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 377482 | PROXIMATE** LINEAR STAPLER | STAPLE, IMPLANTABLE | GDW | ETHICON ENDO-SURGERY, LLC. | NA | G4UD07 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |