FDA Adverse Event Malfunction Summary report: N

AUTO SUTURE ENDO CLIP II M/L

MDR report key: 129284 · Received October 27, 1997

Report

Report Number
1219930-1997-02347
Event Type
Malfunction
Date Received
October 27, 1997
Date of Event
August 22, 1997
Report Date
September 29, 1997
Manufacturer
UNITED STATES SURGICAL CORPORATION
Product Code
GCJ
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MN, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

11/05/1997-SUPPLEMENTAL REPORT #1 SUBMITTED TO FDA.

Description of Event or Problem · 1

THE DEVICE WAS USED DURING A LAPAROSCOPIC CHOLECYSTECTOMY PROCEDURE. REPORTEDLY, THE CLIPS DID NOT LOAD PROPERLY. THE SURGEON USED ANOTHER INSTRUMENT TO COMPLETE THE PROCEDURE. THE HOSP HAS REPORTED NO PT INJURY OCCURRED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 AUTO SUTURE ENDO CLIP II M/L DISPOSABLE CLIP APPLIER GCJ UNITED STATES SURGICAL CORPORATION NA N7E113

Patients

Seq Age Sex Outcome Treatment
1 UNKNOWN