FDA Adverse Event Malfunction Summary report: N

AUTO SUTURE ENDO CLIP*II M/L

MDR report key: 122158 · Received August 22, 1997

Report

Report Number
1219930-1997-02092
Event Type
Malfunction
Date Received
August 22, 1997
Date of Event
August 26, 1997
Report Date
August 26, 1997
Manufacturer
UNITED STATES SURGICAL CORPORATION
Product Code
GCJ
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
JA
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

12/03/1997-SUPPLEMENT REPORT #1 SUBMITTED TO FDA.

Description of Event or Problem · 1

THE DEVICE WAS USED DURING A LAPAROSCOPIC CHOLECYSTECTOMY PROCEDURE. REPORTEDLY, THE STAPLES PREFIRED. 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 N7E69

Patients

Seq Age Sex Outcome Treatment
1 UNKNOWN