FDA Adverse Event Injury Summary report: N

ANGELCHIK PROSTHESIS

MDR report key: 302069 · Received October 26, 2000

Report

Report Number
6000001-2000-00580
Event Type
Injury
Date Received
October 26, 2000
Date of Event
June 6, 1984
Report Date
September 30, 2000
Manufacturer
AMERICAN HEYER-SCHULTE
Product Code
LEI
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
ATTORNEY

Narratives

Description of Event or Problem · 1

CLAIMANT ALLEGES INJURIES AS A RESULT OF AN ANGELCHIK ANTI-REFLUX PROSTHESIS INCLUDING, MIGRATION OF THE ANGELCHIK RING.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 ANGELCHIK PROSTHESIS ANTI-REFLUX PROSTHESIS LEI AMERICAN HEYER-SCHULTE NA 7021240

Patients

Seq Age Sex Outcome Treatment
1 UNKNOWN Other