FDA Adverse Event Injury Summary report: N

INTRALASE

MDR report key: 7371680 · Received March 26, 2018

Report

Report Number
2648035-2018-00417
Event Type
Injury
Date Received
March 26, 2018
Date of Event
February 23, 2018
Report Date
March 26, 2018
Manufacturer
JOHNSON & JOHNSON SURGICAL VISION, INC
Product Code
HNO
PMA / PMN Number
K060372
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
FL, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

(B)(4). FIELD SERVICE SPECIALIST (FSS) VISITED THE ACCOUNT AND CHECKED SYSTEM USING HIS TEST CONES AS THE SITE DID NOT SAVE ANY RELATED TO THE EVENT. HE MEASURED DEPTH IN GEL USING TEST CONES AND FOUND 130 AVERAGE FOR 120 TARGET (WITHIN SPECIFICATION). THEN FSS USED 3 CUSTOMER CONES THAT HAD BEEN USED. ON THE FIRST TWO CONES THE DEPTH WAS 128 (IN RANGE OF THE TEST CONES), THE THIRD CONE MEASURED 111 WHICH IS 20 MICRONS THIN AND NOT IN RANGE. THE CONES THAT HAD SUCTION ISSUES ARE FROM LOT# 60099531. ALL PERTINENT INFORMATION AVAILABLE TO JOHNSON & JOHNSON SURGICAL VISION, INC HAS BEEN SUBMITTED.

Description of Event or Problem · 1

IT WAS REPORTED THAT PATIENTS HAD LASIK PROCEDURE AND HAD VERTICAL GAS BREAKTHROUGH AND FLAP THICKNESS VARIANCES. THE SURGEON USED A BANDAGE CONTACT LENS POST OP. THE ACCOUNT CANNOT PROVIDE HOW MANY PATIENTS WERE AFFECTED. ALL PATIENTS HAD FLAP LIFTED AND EXCIMER TREATMENT WAS COMPLETED. NO PATIENT HAD UNEXPECTED OUTCOME OR NEEDED FURTHER MEDICAL INTERVENTION. NO PATIENT INTERFACE WAS SAVED. THIS REPORT IS FOR THE PATIENT INTERFACE. A SEPARATE REPORTS IS BEING SUBMITTED FOR THE INTRALASE LASER.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
212783 INTRALASE PATIENT INTERFACE HNO JOHNSON & JOHNSON SURGICAL VISION, INC PI-RET UNKNOWN

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention