FDA Adverse Event Malfunction Summary report: N

CA090, DIRECT DRIVE LCA 3/BX

MDR report key: 5010969 · Received August 18, 2015

Report

Report Number
2027111-2015-00566
Event Type
Malfunction
Date Received
August 18, 2015
Date of Event
July 30, 2015
Report Date
August 18, 2015
Manufacturer
APPLIED MEDICAL
Product Code
FZP
PMA / PMN Number
K011236
Removal / Correction Number
Z-1621-2016
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
ZA
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

UPDATE LOT# 1240611. ON (B)(6) 2016, APPLIED MEDICAL ISSUED A VOLUNTARY CLASS II RECALL OF THE CA090 DIRECT DRIVE CLIP APPLIER DUE TO INCREASED CUSTOMER FEEDBACK INDICATING INCONSISTENT CLIP APPLICATION, WHICH HAS THE POTENTIAL TO LEAD TO UNOCCLUDED VESSELS. AN INTERNAL CORRECTIVE ACTION REQUEST HAS BEEN INITIATED TO CONDUCT A THOROUGH INVESTIGATION AND IMPLEMENT APPROPRIATE CORRECTIVE ACTIONS. FDA HAS ISSUED RECALL NUMBER Z-1621-2016 FOR THIS RECALL. IN ACCORDANCE TO 21 CFR 803.56, IF WE OBTAIN ADDITIONAL INFORMATION, WHICH WAS NOT KNOWN OR WAS NOT AVAILABLE WHEN THIS REPORT WAS SUBMITTED, THEN A SUPPLEMENTAL REPORT WILL BE SUBMITTED TO THE FDA.

Additional Manufacturer Narrative · 1

THE INCIDENT DEVICE ANTICIPATED TO RETURN. A FOLLOW-UP REPORT WILL BE PROVIDED UPON COMPLETION OF INVESTIGATION. IN ACCORDANCE TO 21 CFR 803.56, IF WE OBTAIN ADDITIONAL INFORMATION, WHICH WAS NOT KNOWN OR WAS NOT AVAILABLE WHEN THE INITIAL REPORT WAS SUBMITTED, THEN THE SUPPLEMENTAL REPORT WILL BE SUBMITTED TO THE FDA.

Description of Event or Problem · 1

LAP CHOLE - "CLIPS SCISSORING AND JUST SLIDING OFF." PATIENT STATUS - "DISCHARGED."

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
544314 CA090, DIRECT DRIVE LCA 3/BX FZP FZP APPLIED MEDICAL CA090 1240611

Patients

Seq Age Sex Outcome Treatment
1