ACRYSOF RESTOR
Report
- Report Number
- 1119421-2012-01028
- Event Type
- Injury
- Date Received
- August 17, 2012
- Date of Event
- October 19, 2010
- Report Date
- July 17, 2012
- Manufacturer
- ALCON RESEARCH, LTD. / HUNTINGTON
- Product Code
- HQL
- PMA / PMN Number
- P040020
- Removal / Correction Number
- NA
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- TX, US
- Reporter Occupation
- OTHER
Narratives
THE PRODUCT WAS NOT RETURNED FOR ANALYSIS. THE PRODUCT HISTORY RECORDS COULD NOT BE REVIEWED BECAUSE THE REPORTING FACILITY DID NOT PROVIDE A LOT NUMBER OR ANY IDENTIFICATION TRACEABLE TO THE MFG DOCUMENTATION. THE PRODUCT INVESTIGATION COULD NOT IDENTIFY A ROOT CAUSE. NOT ENOUGH INFO WAS PROVIDED FROM THE ACCOUNT TO PROPERLY COMPLETE AN INVESTIGATION. ADD'L INFO WAS REQUESTED BY PHONE, FAX AND MAIL. A COMPLETED QUESTIONNAIRE WAS REC'D. ROENSCH A, CHARTON J, BLOMQUIST P, AGGARWAL N, MCCULLEY J. RESIDENT EXPERIENCE WITH TORIC AND MULTIFOCAL INTRAOCULAR LENSES IN A PUBLIC COUNTY HOSPITAL SYSTEM. J CATARACT REFRACT SURG 2012; 38:793. (B)(4).
IN A JOURNAL ARTICLE, THE AUTHORS PRESENTED THE OUTCOMES OF TORIC AND MULTIFOCAL INTRAOCULAR LENS (IOL) IMPLANT PROCEDURES PERFORMED BY THE RESIDENT SURGEONS. FOR THIS PT, THE INVESTIGATOR REPORTED AN UNEXPECTED POSTOPERATIVE OUTCOME FOLLOWING INTRAOCULAR LENS (IOL) IMPLANT SURGERY. HE ALSO DOES NOT FEEL THE IOL CAUSED OR CONTRIBUTED TO THE EVENT. ADD'L INFO WAS REC'D FROM THE CORRESPONDING AUTHOR WHO INDICATED THAT THERE WAS NO TREATMENT FOR THIS PT AND THE EVENT CONTINUES. THERE ARE NINE MEDICAL DEVICE REPORTS ASSOCIATED WITH THIS EVENT. THIS REPORT IS FOR FIFTH PT, RIGHT EYE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | ACRYSOF RESTOR | INTRAOCULAR LENS | HQL | ALCON RESEARCH, LTD. / HUNTINGTON | SN6AD1 | UNK |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 80 YR | Other | DUOVISC| AND CARTRIDGE| MONARCH HANDPIECE |