MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a user facility report with the FDA on 2018-12-19 for CRYSTALENS ACCOMMODATING IOL manufactured by Bausch + Lomb.
        [130884358]
Investigation of this event is in progress. A follow-up report will be submitted upon completion of the investigation.
 Patient Sequence No: 1, Text Type: N, H10
        [130884359]
A physician reported to have observed glare/tilt of an implanted lens in the patient's left eye. The physician referred the patient to a retina specialist, who then decided to explant the lens. Additional information has been requested, but has not been received.
 Patient Sequence No: 1, Text Type: D, B5
| Report Number | 0001313525-2018-00240 | 
| MDR Report Key | 8180182 | 
| Report Source | USER FACILITY | 
| Date Received | 2018-12-19 | 
| Date of Report | 2018-11-28 | 
| Date of Event | 2018-10-17 | 
| Date Added to Maude | 2018-12-19 | 
| Event Key | 0 | 
| Report Source Code | Manufacturer report | 
| Manufacturer Link | Y | 
| Number of Patients in Event | 0 | 
| Adverse Event Flag | 3 | 
| Product Problem Flag | 3 | 
| Reprocessed and Reused Flag | 3 | 
| Health Professional | 3 | 
| Initial Report to FDA | 3 | 
| Report to FDA | 3 | 
| Event Location | 3 | 
| Manufacturer Contact | MS. TES PROUD | 
| Manufacturer Street | 1400 NORTH GOODMAN STREET | 
| Manufacturer City | ROCHESTER NY 14609 | 
| Manufacturer Country | US | 
| Manufacturer Postal | 14609 | 
| Manufacturer Phone | 5853388549 | 
| Manufacturer G1 | BAUSCH + LOMB | 
| Manufacturer Street | 21 NORTH PARK PLACE BLVD. | 
| Manufacturer City | CLEARWATER FL 33759 | 
| Manufacturer Country | US | 
| Manufacturer Postal Code | 33759 | 
| Single Use | 3 | 
| Previous Use Code | 3 | 
| Event Type | 3 | 
| Type of Report | 3 | 
| Brand Name | CRYSTALENS ACCOMMODATING IOL | 
| Generic Name | LENS, INTRAOCULAR, ACCOMMODATIVE | 
| Product Code | NAA | 
| Date Received | 2018-12-19 | 
| Operator | HEALTH PROFESSIONAL | 
| Device Availability | N | 
| Device Age | DA | 
| Device Eval'ed by Mfgr | R | 
| Device Sequence No | 1 | 
| Device Event Key | 0 | 
| Manufacturer | BAUSCH + LOMB | 
| Manufacturer Address | 1400 NORTH GOODMAN STREET ROCHESTER NY 14609 US 14609 | 
| Patient Number | Treatment | Outcome | Date | 
|---|---|---|---|
| 1 | 0 | 1. Other | 2018-12-19 |