FDA Adverse Event
Malfunction
Summary report: N
POSTERIOR CHAMBER INTRAOCULAR LENS
MDR report key: 1052770
·
Received May 23, 2008
Report
- Report Number
- 1920664-2008-00595
- Event Type
- Malfunction
- Date Received
- May 23, 2008
- Date of Event
- April 29, 2008
- Report Date
- April 29, 2008
- Manufacturer
- BAUSCH & LOMB, INC.
- Product Code
- HQL
- PMA / PMN Number
- P840039
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- OH, US
- Reporter Occupation
- UNKNOWN
Narratives
Additional Manufacturer Narrative · 1
(OTHER) - LENS HAPTIC.
Description of Event or Problem · 1
THE HAPTIC OF THE LENS WAS FOUND BENT UPON OPENING THE LENS CARRIER.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | POSTERIOR CHAMBER INTRAOCULAR LENS | INTRAOCULAR LENS | HQL | BAUSCH & LOMB, INC. |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |