FDA Adverse Event
Injury
Summary report: N
HERRICK LACRIMAL PLUG
MDR report key: 539008
·
Received August 12, 2004
Report
- Report Number
- 2024818-2004-00002
- Event Type
- Injury
- Date Received
- August 12, 2004
- Report Date
- July 12, 2004
- Manufacturer
- LACRIMEDICS, INC.
- Product Code
- LZU
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Occupation
- ATTORNEY
Narratives
Description of Event or Problem · 1
DR REPORTED THAT HE HAD A PT HE WAS HAVING TROUBLE IRRIGATING PLUGS OUT OF. PT EVENTUALLY HAD A DCR. DR HAS NOT SUPPLIED ANY FURTHER INFO.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | HERRICK LACRIMAL PLUG | INTRACANILICULAR PLUG | LZU | LACRIMEDICS, INC. | NI | NI |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | * | Required Intervention |