FDA Adverse Event Injury Summary report: N

AKREOS ADVANCED OPTICS ASPHERIC LENS

MDR report key: 3132995 · Received May 23, 2013

Report

Report Number
1119279-2013-00163
Event Type
Injury
Date Received
May 23, 2013
Date of Event
April 22, 2013
Report Date
April 23, 2013
Manufacturer
BAUSCH & LOMB
Product Code
HQL
PMA / PMN Number
P060022
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
PA, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Additional Manufacturer Narrative · 1

THE LENS WAS RETURNED TO B+L. VISUAL INSPECTION FOUND THE RETURNED LENS IS NOT DAMAGED. A FUNCTIONAL TESTING WAS PERFORMED USING A SAMPLE DELIVERY DEVICE. THE LENS LOADED AND DELIVERED WITHOUT DIFFICULTY. THE DEVICE HISTORY RECORDS WERE REVIEWED AND THERE WERE NO DISCREPANCIES OR UNUSUAL FINDINGS THAT RELATE TO THE REPORTED ISSUE. BASED ON THE INFO AVAILABLE, THE EXACT CAUSE OF THE REPORTED EVENT COULD NOT BE CONCLUSIVELY DETERMINED. HOWEVER, ACCORDING TO THE SURGEON, THE MOST LIKELY CAUSE OF THE EVENT WAS A PRE-EXISTING PT CONDITION WHICH RESULTED FROM AN INTRAVITREAL INJECTION. SEE SCANNED PAGE.

Description of Event or Problem · 1

IT WAS REPORTED THAT THE LENS WAS INTRAOPERATIVELY REMOVED FROM THE PT'S LEFT EYE DUE TO A POSTERIOR CAPSULE DEFECT. ACCORDING TO THE SURGEON, THE CAPSULE DEFECT WAS MOST LIKELY A PRE-EXISTING PT CONDITION (CAPSULE DEFECT) WHICH RESULTED FROM AN INTRAVITREAL INJECTION. THE PRE-EXISTING DEFECT ENLARGED AFTER THE IOL WAS INSERTED INTO THE BAG. VITRECTOMY WAS PERFORMED AND AN LI61 INTRAOCULAR LENS WAS PLACED IN THE SULCUS AS A REPLACEMENT. PLEASE REFERENCE MDR#: 1119279-2013-00164 FOR THE DELIVERY DEVICE USED DURING THE EVENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
229220 AKREOS ADVANCED OPTICS ASPHERIC LENS HQL/INTRAOCULAR LENS HQL BAUSCH & LOMB AO60G 1230204

Patients

Seq Age Sex Outcome Treatment
1 71 YR Other AI-28 DELIVERY SYSTEM