CEEON
Report
- Report Number
- 2648035-2016-00859
- Event Type
- Injury
- Date Received
- June 3, 2016
- Report Date
- November 28, 2016
- Manufacturer
- ABBOTT MEDICAL OPTICS
- Product Code
- HQL
- PMA / PMN Number
- P990080
- Adverse Event
- Yes
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- GB
- Reporter Occupation
- PHYSICIAN
Narratives
THE INTRAOCULAR LENS (IOL) WAS NOT RETURNED TO THE MANUFACTURER FOR EVALUATION; THEREFORE PRODUCT TESTING COULD NOT BE PERFORMED AND THE CUSTOMER'S REPORTED COMPLAINT COULD NOT BE VERIFIED. MANUFACTURING RECORDS REVIEW: THE MANUFACTURING RECORDS COULD NOT BE REVIEWED SINCE THE SERIAL NUMBER IS UNKNOWN/NOT PROVIDED. ALL PERTINENT INFORMATION AVAILABLE TO ABBOTT MEDICAL OPTICS HAS BEEN SUBMITTED.
UDI #: UNKNOWN SINCE SERIAL NUMBER WAS NOT PROVIDED DATE OF EVENT: UNKNOWN, NOT PROVIDED. CATALOG #, EXPIRATION DATE, AND SERIAL #: UNKNOWN, NOT PROVIDED. WHAT IS KNOWN IS THE LENS WAS A +24.5 DIOPTER. IMPLANT DATE: IF IMPLANTED, GIVE DATE: UNKNOWN, NOT PROVIDED. EXPLANT DATE: IF EXPLANTED, GIVE DATE: NOT APPLICABLE AS THE LENS REMAINS IMPLANTED PER THE ARTICLE. INITIAL REPORTER PHONE NUMBER: UNKNOWN, NOT PROVIDED. MFG DATE: DEVICE MANUFACTURE DATE: UNKNOWN SINCE SERIAL NUMBER IS UNKNOWN. ALL PERTINENT INFORMATION AVAILABLE TO ABBOTT MEDICAL OPTICS HAS BEEN SUBMITTED.
THE ''BILATERAL RUPTURE OF THE POSTERIOR CAPSULE AND INTRAOCULAR LENS DISLOCATION FROM EXCESSIVE EYE RUBBING'' ARTICLE WAS REVIEWED. AUTHOR(S): RAMY BASSILY, BM, FRCOPHTH, ANNA LENCOVA, MD, PHD, FEBO, MADHAVAN S. RAJAN, MB BS, MS, MD, FRCOPHTH PUBLICATION: J CATARACT REFRACT SURG 2016; 42:329-331 CROWN COPYRIGHT Q 2016 PUBLISHED BY ELSEVIER INC. ON BEHALF OF ASCRS AND ESCRS. ALL RIGHTS RESERVED. HTTP://DX.DOI.ORG/10.1016/J.JCRS.2016.01.01. THE ARTICLE REPORTED AN UNUSUAL CASE OF A (B)(6)-YEAR-OLD WOMAN WITH SEVERE ATOPIC ECZEMA WHO DEVELOPED SUDDEN-ONSET REDUCTION OF VISION IN THE RIGHT EYE FOLLOWING EXCESSIVE EYE RUBBING 9 YEARS AFTER CATARACT SURGERY. EXAMINATION IDENTIFIED POSTERIOR CAPSULE RUPTURE WITH DISLOCATION OF THE INTRAOCULAR LENS (IOL) POSTERIORLY INTO THE VITREOUS CAVITY IN THE RIGHT EYE AND POSTERIOR CAPSULE RUPTURE WITH MILD DISLOCATION OF THE IOL IN THE BAG IN THE LEFT EYE. TO THE AUTHORS' KNOWLEDGE, THIS WAS THE FIRST REPORTED CASE OF SIMULTANEOUS BILATERAL POSTERIOR CAPSULE RUPTURE FOLLOWING UNEVENTFUL SURGERY AND SECONDARY TO EYE RUBBING. SILICONE INTRAOCULAR LENSES, MODEL CEEON 911A, WERE IMPLANTED IN BOTH EYES: A +24.5 DIOPTER (D) LENS IN THE LEFT EYE AND A +26.5 D LENS IN THE RIGHT EYE. THE CAUSE OF THE CATARACTS WAS THOUGHT TO BE THE USE OF LONG-TERM SYSTEMIC STEROIDS TO CONTROL ATOPY AND SEVERE ECZEMA. THE PATIENT HAD NO HISTORY OF CONGENITAL CATARACTS, TRAUMA, OR CONNECTIVE TISSUE DISORDERS. THE ATOPY HAD REQUIRED LONG COURSES OF IMMUNOSUPPRESSION WITH STEROIDS, SYSTEMIC CYCLOSPORINE, AND AZATHIOPRINE THROUGHOUT HER LIFE. AT THE TIME OF PRESENTATION, THE PATIENT WAS TAKING A COURSE OF ORAL METHYLPREDNISOLONE FOR A FLARE-UP OF THE ECZEMA. THE PREVIOUSLY RECORDED CORRECTED PSEUDOPHAKIC VISUAL ACUITY WAS 6/6 SNELLEN IN BOTH EYES. SINCE BOTH EYES WERE AFFECTED, A SEPARATE MDR WILL BE FILED FOR EACH EYE. THIS MDR IS FOR THE LEFT EYE WITH A 24.5 DIOPTER 911A LENS. EXAMINATION OF THE LEFT EYE SHOWED A RUPTURED POSTERIOR CAPSULE WITH MILD DECENTRATION OF THE IOL IN THE CAPSULAR BAG; THE CDVA WAS 6/6. THE LEFT EYE IS UNDERGOING PERIODIC OBSERVATION. THE MECHANISM OF THE POSTERIOR CAPSULE TEAR COULD HAVE BEEN FOCAL DIGITAL PRESSURE ON THE EYE THAT DISPLACED THE IOL VERTICALLY, CAUSING THE SHARP EDGE OF THE HAPTIC TO RUPTURE THE POSTERIOR CAPSULE. NO ADDITIONAL INFORMATION WAS PROVIDED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 352542 | CEEON | MONOFOCAL IOLS | HQL | ABBOTT MEDICAL OPTICS | 911A |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 36 YR | Other |