FDA Adverse Event Other Summary report: N

*

MDR report key: 509018 · Received January 14, 2004

Report

Report Number
MW1030890
Event Type
Other
Date Received
January 14, 2004
Date of Event
December 9, 2003
Report Date
January 13, 2004
Manufacturer
*
Product Code
LMO
Adverse Event
Yes
Report Source
Voluntary report
Reporter Location
FL, US
Reporter Occupation
RISK MANAGER

Narratives

Description of Event or Problem · 1

RUPTURED GLOBE AFTER PKP TRANSPLANT OF CORNEA TISSUE FOR A REPAIR OF RUPTURED GLOBE AND REPAIR OF IRIS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 * CORNEA TISSUE LMO * * *

Patients

Seq Age Sex Outcome Treatment
1 * Other