FDA Adverse Event Malfunction Summary report: N

IDRIVE ULTRA POWERED HANDLE 1

MDR report key: 4163650 · Received October 10, 2014

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

Additional Manufacturer Narrative · 1

TRACKING NUMBERS: REFERENCE US201409-0829, US201409-0902 AND US201409-0903 AS THE INCIDENT DESCRIBES 3 DIFFERENT PROCEDURES.

Additional Manufacturer Narrative · 1

(B)(4).

Description of Event or Problem · 1

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,