FDA Adverse Event Other Summary report: N

HERRICK LACRIMAL PLUG

MDR report key: 476733 · Received August 8, 2003

Report

Report Number
2024818-2003-00002
Event Type
Other
Date Received
August 8, 2003
Date of Event
April 10, 2002
Report Date
August 8, 2003
Manufacturer
LACRIMEDICS, INC.
Product Code
LZU
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Occupation
INVALID DATA

Narratives

Description of Event or Problem · 1

PT HAD PLUGS PUT IN IN 1998. SINCE THEN HAD THEM IRRIGATED OUT. ONE PLUG REMAINS DUE TO A BLOCKAGE IN THE LOWER RIGHT DUCT. THE PT CONTINUES TO SUFFER CONSTANT TEARING.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 HERRICK LACRIMAL PLUG INTRACANILICULAR PLUG LZU LACRIMEDICS, INC. * *

Patients

Seq Age Sex Outcome Treatment
1 * Other