INTRALASE
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
(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.
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 |