FDA Adverse Event Malfunction Summary report: N

WECK HEMOLOK L CLIPS 6/CART 84/BOX

MDR report key: 4180345 · Received October 15, 2014

Report

Report Number
3003898360-2014-00824
Event Type
Malfunction
Date Received
October 15, 2014
Date of Event
August 1, 2014
Report Date
September 15, 2014
Manufacturer
TELEFLEX
Product Code
MCH
Report Source
Manufacturer report
Reporter Location
FR
Reporter Occupation
NOT APPLICABLE

Narratives

Additional Manufacturer Narrative · 1

A DEVICE HISTORY RECORD (DHR) REVIEW DID NOT SHOW ISSUES RELATED TO COMPLAINT. THE COMPLAINT CANNOT BE CONFIRMED SINCE THE SAMPLE WAS NOT RETURNED. THE MFR WILL CONTINUE TO MONITOR AND TREND RELATING COMPLAINTS.

Description of Event or Problem · 1

ALLEGED ISSUE: DURING A LAPAROSCOPIC RIGHT SURRENALECTOMY (ADRENALECTOMY) SURGERY, THE PRINCIPAL SURRENAL VEIN WAS LOCATED TO BE SECTION BETWEEN 2 CLIPS. THE CLIPS IN THIS CARTRIDGE DID NOT WORK, THEY DID NOT CLOSE. THE PT'S CONDITION IS FINE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
656229 WECK HEMOLOK L CLIPS 6/CART 84/BOX LIGATING CLIPS MCH TELEFLEX 01B1400269

Patients

Seq Age Sex Outcome Treatment
1