FDA Adverse Event Injury Summary report: N

CRYSTALENS ACCOMMODATING IOL

MDR report key: 5099284 · Received September 23, 2015

Report

Report Number
0001313525-2015-02629
Event Type
Injury
Date Received
September 23, 2015
Date of Event
June 11, 2015
Report Date
August 26, 2015
Manufacturer
BAUSCH & LOMB INCORPORATED
Product Code
NAA
PMA / PMN Number
P030002
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
VA, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE LENS REMAINED IMPLANTED. ONE RETAIN SAMPLE FROM THE SAME LOT (022096) WAS DIMENSIONALLY INSPECTED AND ALL MEASUREMENTS WERE FOUND TO BE WITHIN SPECIFICATIONS. THE DEVICE HISTORY RECORDS WERE REVIEWED AND THERE WERE NO DISCREPANCIES OR UNUSUAL FINDING THAT RELATE TO THE REPORTED ISSUE. BASED ON THE INFORMATION AVAILABLE, THE ROOT CAUSE OF THE REPORTED EVENT COULD NOT BE CONCLUSIVELY DETERMINED.

Additional Manufacturer Narrative · 1

INVESTIGATION OF THIS EVENT IS IN PROGRESS. A SUPPLEMENTAL REPORT WILL BE SUBMITTED UPON COMPLETION OF THE INVESTIGATION.

Description of Event or Problem · 1

IT WAS REPORTED THAT APPROXIMATELY 1 MONTH POST LENS IMPLANT THE PATIENT NOTED BLURRED VISION. THE LENS VAULTED (Z-SYNDROME). POSTERIOR CAPSULAR OPACIFICATION (PCO) WAS ALSO OBSERVED. A YAG WAS PERFORMED BUT WAS UNSUCCESSFUL. THE REASON FOR YAG WAS NOT PROVIDED. THE LENS WAS SUBSEQUENTLY REPOSITIONED. THE PATIENT'S CURRENT PROGNOSIS AND TREATMENT WERE DESCRIBED AS "GOOD, ADJUST GLAUCOMA DROPS".

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
629591 CRYSTALENS ACCOMMODATING IOL LENS, INTRAOCULAR, ACCOMMODATIVE NAA BAUSCH & LOMB INCORPORATED AT50AO 022096

Patients

Seq Age Sex Outcome Treatment
1 69 YR Other