FDA Adverse Event Injury Summary report: N

CATALYS PRECISION LASER SYSTEM

MDR report key: 3908248 · Received June 5, 2014

Report

Report Number
3005675890-2014-00020
Event Type
Injury
Date Received
June 5, 2014
Date of Event
May 8, 2014
Report Date
June 5, 2014
Manufacturer
OPTIMEDICA CORPORATION
Product Code
OOE
PMA / PMN Number
K121091
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
FL, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

INVESTIGATION OF THIS INCIDENT INCLUDED ANALYSIS OF THE SYSTEM DATABASE AND THE SYSTEM OPTICAL COHERENCE TOMOGRAPHY (OCT) RECORDING. THE SYSTEM VIDEO DISPLAY RECORDING AND THE OPERATING ROOM SURGICAL VIDEO WERE NOT AVAILABLE FOR ANALYSIS. FROM THE ANALYSIS OF THE SYSTEM DATABASE AND THE SYSTEM OCT RECORDING THERE WERE NO SYSTEM RELATED ANOMALIES OBSERVED AND ALL SETTINGS AND PARAMETERS OF THE SYSTEM WERE FOUND TO BE WITHIN ACCEPTABLE LIMITS. THE SYSTEM DATABASE VIDEO IMAGES INDICATED THE ABSENCE OF, OR MINIMAL, EYE MOVEMENT DURING THE LASER TREATMENT. THE SURGEON STATED STANDARD CONTINUOUS CURVILINEAR CAPSULORHEXIS (CCC) SURGICAL TECHNIQUE WAS USED TO REMOVE THE CAPSULOTOMY DISC AND PHACOEMULSIFICATION WAS USED TO EXTRACT THE CATARACT. THE CATALYST SYSTEM PERFORMED AS DESIGNED; HOWEVER THE CAUSE (S) OF THE ANTERIOR CAPSULE TEAR IS UNK.

Description of Event or Problem · 1

IT WAS REPORTED THAT A PT WHO UNDERWENT ANTERIOR CAPSULOTOMY, LENS FRAGMENTATION, AND CORNEAL INCISIONS WITH THE CATALYST SYSTEM (SYSTEM) SUBSEQUENTLY EXPERIENCED AN ANTERIOR CAPSULE TEAR IN THE OPERATING ROOM (O.R.) DURING THE SURGICAL PROCEDURE TO REMOVE THE CATARACT. THE SURGEON DID OBSERVE A TAG DURING REMOVAL OF THE CAPSULOTOMY. NO ADDITIONAL COMPLICATION AND/OR MEDICAL INTERVENTION WERE REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
329441 CATALYS PRECISION LASER SYSTEM OPHTHALMIC FEMTOSECOND LASER OOE OPTIMEDICA CORPORATION CATALYS-U

Patients

Seq Age Sex Outcome Treatment
1 67 YR Other