FDA Adverse Event Malfunction Summary report: N

LIGACLIP MULTIPLE CLIP APPLIER

MDR report key: 243950 · Received October 11, 1999

Report

Report Number
1527736-1999-05296
Event Type
Malfunction
Date Received
October 11, 1999
Report Date
September 16, 1999
Manufacturer
LACEY MFG CO.
Product Code
GDO
Removal / Correction Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CO, US
Reporter Occupation
NURSE

Narratives

Description of Event or Problem · 1

IT WAS REPORTED BY THE REP THAT THE (1) EMS AND THE (1) MCM20 WERE USED DURING AN UNK PROCEDURE, BY AN UNK SURGEON, ON AN UNK DATE. THE ONLY INFO GIVEN IS THAT THE DEVICES MISFIRED. THERE WAS NO CONSEQUENCE TO THE PT. THERE IS NO OTHER INFO AVAILABLE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 LIGACLIP MULTIPLE CLIP APPLIER CLIP APPLIER GDO LACEY MFG CO. NA M4EW35

Patients

Seq Age Sex Outcome Treatment
1 UNKNOWN Other