FDA Adverse Event Malfunction Summary report: N

AUTO SUTURE TA PREMIUM SURGICLIP M-9.75

MDR report key: 93569 · Received May 23, 1997

Report

Report Number
2647580-1997-00530
Event Type
Malfunction
Date Received
May 23, 1997
Date of Event
April 1, 1997
Report Date
April 24, 1997
Manufacturer
UNITED STATES SURGICAL CORP.
Product Code
GDO
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
PA, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

6/23/1997-SUPPLEMENTAL REPORT #1 SUBMITTED TO FDA.

Description of Event or Problem · 1

DURING AN UNSPECIFIED PROCEDURE, THE CLIPS DID NOT FORM PROPERLY. THE SURGEON APPLIED ANOTHER DEVICE WITHOUT PT INJURY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 AUTO SUTURE TA PREMIUM SURGICLIP M-9.75 DISPOSABLE CLIP APPLIER GDO UNITED STATES SURGICAL CORP. NA P6H381

Patients

Seq Age Sex Outcome Treatment
1 UNKNOWN