FDA Adverse Event
Injury
Summary report: N
TORIC LENS
MDR report key: 2181272
·
Received July 15, 2011
Report
- Report Number
- MW5021485
- Event Type
- Injury
- Date Received
- July 15, 2011
- Manufacturer
- UNK
- Product Code
- MJP
- Adverse Event
- Yes
- Report Source
- Voluntary report
- Reporter Occupation
- PATIENT
Narratives
Description of Event or Problem · 1
SINCE HAVING TORIC LENS IMPLANTS, I HAVE HAD A LOT OF "CRINKLING" AS DESCRIBED BY DR. ALSO L EYE HAS FLOATING LIGHTS WHEN CLOSING EYES. OCCASIONALLY SEE SMALL HALOS. THESE SIDE EFFECTS NOTED ONLY AFTER IMPLANTS. DIAGNOSIS OR REASON FOR USE: LENS IMPLANTS TO HELP ASTIGMATISM DONE AS PT HAD CATARACTS.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | TORIC LENS | TORIC LENS | MJP | UNK |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 64 YR |