FDA Adverse Event Injury Summary report: N

HYDROVIEW INTRAOCULAR LENS

MDR report key: 1083500 · Received July 28, 2008

Report

Report Number
1920664-2008-00780
Event Type
Injury
Date Received
July 28, 2008
Date of Event
May 21, 2008
Report Date
July 1, 2008
Manufacturer
BAUSCH & LOMB
Product Code
HQL
PMA / PMN Number
P990014
Product Problem
Yes
Report Source
Manufacturer report
Reporter Occupation
PHYSICIAN

Narratives

Description of Event or Problem · 1

THE LENS WAS EXPLANTED DUE TO OPACIFICATION.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 HYDROVIEW INTRAOCULAR LENS INTRAOCULAR LENS HQL BAUSCH & LOMB

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention