IDRIVE ULTRA POWERED HANDLE 1
Report
- Report Number
- 1219930-2014-00932
- Event Type
- Malfunction
- Date Received
- October 10, 2014
- Report Date
- September 15, 2014
- Manufacturer
- COVIDIEN, FORMERLY US SURGICAL A DIVISON
- Product Code
- GDW
- PMA / PMN Number
- K121510
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- GM
- Reporter Occupation
- NURSE
Narratives
TRACKING NUMBERS: REFERENCE US201409-0829, US201409-0902 AND US201409-0903 AS THE INCIDENT DESCRIBES 3 DIFFERENT PROCEDURES.
(B)(4).
THE INSTRUMENT DID NOT FIRE DURING 3 DIFFERENT PROCEDURES WITH 3 DIFFERENT SURGEONS (ALWAYS SAME IDRIVE WITH SAME ADAPTER). NO PATIENT HARM. NO PATIENT INJURED, NO EXTENSION OF INCISION OR SURGERY TIME, NO BLOOD LOSS, NO TISSUE DAMAGE, NO CHANGE OF PROCEDURE, NO PART FELL INTO CAVITY, NO REINFORCEMENT MATERIAL USED. ADDITIONAL INFORMATION REQUESTED VIA EMAIL 1. PLEASE CONFIRM THAT PRODUCT WILL BE RETURNED FOR INVESTIGATION. 2. DID ALL PROCEDURES OCCUR ON THE SAME DATE? 3. DID THE DEVICE FUNCTION PROPERLY AFTER THE INITIAL MALFUNCTION? A) IF NOT, WHAT WAS THE DONE TO COMPLETE THE PROCEDURE? 4. WHAT ARE THE STATUS LIGHTS DISPLAYING ON THE I-DRIVE? 5. WHAT IS THE PRODUCT ID AND LOT NUMBER FOR THE RELOAD USED WITH THIS STAPLER? IF THE CUSTOMER CANNOT SUPPLY THE PRODUCT ID OR LOT NUMBER, WAS THE RELOAD A UNIVERSAL ROTICULATOR SULU, A STRAIGHT SULU, OR A TRI-STAPLE RELOAD? 6. WHAT IS THE PATIENT AGE, WEIGHT, GENDER? 7. WHAT IS THE LAST KNOWN PATIENT STATUS?
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 639304 | IDRIVE ULTRA POWERED HANDLE 1 | REUSABLE SURGICAL STAPLER | GDW | COVIDIEN, FORMERLY US SURGICAL A DIVISON | IDRVULTRA1 | N4D1306UX |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | EGIAADAPT, ENDO GIA ADAPTER STANDARD, |