FDA Adverse Event Injury Summary report: N

IFS

MDR report key: 7493632 · Received May 8, 2018

Report

Report Number
3006695864-2018-01025
Event Type
Injury
Date Received
May 8, 2018
Date of Event
April 10, 2018
Report Date
May 8, 2018
Manufacturer
JOHNSON & JOHNSON SURGICAL VISION, INC
Product Code
HNO
UDI-DI
05050474573468
PMA / PMN Number
K060372
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
OH, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

(B)(4). A REVIEW OF RECORDS RELATED TO THE DEVICE INCLUDING LABELING, COMPLAINT TRENDING, AND RISK DOCUMENTATION WILL BE PERFORMED. UPON COMPLETION OF THIS REVIEW, IF THERE IS ANY FURTHER RELEVANT INFORMATION OBTAINED, A SUPPLEMENTAL MEDWATCH WILL BE FILED. ALL PERTINENT INFORMATION AVAILABLE TO JOHNSON & JOHNSON SURGICAL VISION, INC HAS BEEN SUBMITTED.

Description of Event or Problem · 1

IT WAS REPORTED THAT A LASER VISION CORRECTION PATIENT HAD SURGERY ON (B)(6) 2018 AND PRESENTED ON (B)(6) 2018 WITH TRANSIENT LIGHT SENSITIVITY SYNDROME THAT STARTED SHORTLY AFTER TREATMENT IN BOTH EYES. THE TOPICAL STEROID DOSAGE WAS INCREASED (LOTEMAX GEL 3 TIMES A DAY FOR 7 DAYS THEN TAPER). IT WAS STATED THAT THE PATIENT HAD NO LOSS OF BEST CORRECTED VISUAL ACUITY (BCVA). THE PATIENT COMPLAINED OF PHOTOPHOBIA THAT MAKES DIFFICULT WATCHING MOVIES AT THEATER, SITTING UNDER BRIGHT LIGHTS INDOORS AND CAR HEADLIGHTS APPEAR LIKE HIGH BEAMS ON - RIGHT EYE MORE THAN LEFT EYE. PATIENT REPORTED IS HAPPY WITH VISION AND SYMPTOMS ARE NOT INTERFERING WITH DAILY ACTIVITIES. BCVA FROM (B)(6) 2018: RIGHT EYE PRE-OP 20/20 -.50 X -1.75 X 62, LEFT EYE PRE-OP 20/20 .00 X -1.25 X 162. BCVA FROM (B)(6) 2018: RIGHT EYE POST-OP 20/20 .00 X .00 X 90, LEFT EYE POST-OP 20/20 -1.50 X -.50 X 90.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
338243 IFS FEMTOSECOND LASER HNO JOHNSON & JOHNSON SURGICAL VISION, INC J20007D 05050474573468

Patients

Seq Age Sex Outcome Treatment
1 51 YR Required Intervention WAVELIGHT (B)(4)