FDA Adverse Event Injury Summary report: N

HERRICK LACRIMAL PLUG

MDR report key: 376272 · Received February 8, 2002

Report

Report Number
2024818-2002-00002
Event Type
Injury
Date Received
February 8, 2002
Date of Event
October 30, 2001
Report Date
February 5, 2002
Manufacturer
LACRIMEDICS, INC.
Product Code
LZU
Removal / Correction Number
NA
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Occupation
INVALID DATA

Narratives

Description of Event or Problem · 1

HERRICK PLUG ALLEGEDLY EMBEDDED IN CANALICULUS OF BOTH LOWER LIDS REQUIRING A SURGICAL PROCEDURE (I.E. DCR) TO REMOVE. OCULOPLAST ATTEMPTED TO REMOVE PLUG(S) WITH PRESSURE IRRIGATION PRIOR TO SURGERY WITHOUT APPARENT SUCCESS. ONE PLUG WAS RECOVERED EMBEDDED IN SCAR TISSUE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 HERRICK LACRIMAL PLUG INTRACANALICULAR LACRIMAL PLUG LZU LACRIMEDICS, INC. HLP3 UNK

Patients

Seq Age Sex Outcome Treatment
1 49 YR Required Intervention