FDA Adverse Event Malfunction Summary report: N

AUTO SUTURE ENDO CLIP 10MM REUSABLE

MDR report key: 126361 · Received October 8, 1997

Report

Report Number
1219161-1997-01397
Event Type
Malfunction
Date Received
October 8, 1997
Report Date
September 11, 1997
Manufacturer
UNITED STATES SURGICAL CORP.
Product Code
GCJ
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
UK
Reporter Occupation
NURSE

Narratives

Additional Manufacturer Narrative · 1

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

Description of Event or Problem · 1

THE PRODUCT WAS USED DURING AN UNSPECIFIED PROCEDURE. REPORTEDLY, THE CLIPS SCISSORED. THE HOSP HAS REPORTED NO PT INJURY OCCURRED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 AUTO SUTURE ENDO CLIP 10MM REUSABLE SURGICAL STAPLING INSTRUMENT GCJ UNITED STATES SURGICAL CORP. 176599 NA

Patients

Seq Age Sex Outcome Treatment
1 UNKNOWN