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 |