STAR
Report
- Report Number
- 3006695864-2018-00585
- Event Type
- Injury
- Date Received
- March 26, 2018
- Date of Event
- February 26, 2018
- Report Date
- April 26, 2018
- Manufacturer
- JOHNSON & JOHNSON SURGICAL VISION, INC
- Product Code
- LZS
- UDI-DI
- 00(01)(21)5330
- PMA / PMN Number
- P930016
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- TX, US
- Reporter Occupation
- PHYSICIAN
Narratives
MANUFACTURER YEAR 2003. ALL PERTINENT INFORMATION AVAILABLE TO JOHNSON & JOHNSON SURGICAL VISION, INC. HAS BEEN SUBMITTED.
A REVIEW OF THE RECORDS RELATED TO THE DEVICE THAT INCLUDED LABELING, MANUALS, TRENDING, AND RISK DOCUMENTATION WAS PERFORMED. THE TREND REVIEW SHOWS THAT THERE IS NO SIGNIFICANT CHANGE OVER HISTORICAL COMPLAINT LIMITS AND NO RECOGNIZABLE ADVERSE TREND. THE RISKS AND MITIGATIONS ASSOCIATED WITH THE COMPLAINT ISSUE ARE IDENTIFIED IN EXISTING RISK DOCUMENTS AND NO NEW RISKS WERE IDENTIFIED AS PART OF THIS INVESTIGATION. THERE WAS NO PRODUCT DEFICIENCY IDENTIFIED. ALL PERTINENT INFORMATION AVAILABLE TO JOHNSON & JOHNSON SURGICAL VISION, INC. HAS BEEN SUBMITTED.
THE SURGERY CENTER REPORTED THAT A LASER VISION CORRECTION PATIENT EXPERIENCED FUZZY VISION, FLUCTUATION, AND FOREIGN BODY SENSATION IN THE RIGHT EYE (OD) AT THE 2-DAY POST OP EXAM. ORAL STEROIDS (PREDNISONE) WERE PRESCRIBED AND TOPICAL STEROID DOSAGE WAS INCREASED TO RESOLVE SYMPTOMS. BEST CORRECTED VISUAL ACUITY (BCVA) FROM (B)(6) 2017: RIGHT EYE PRE-OP 20/20 -.25 X -.75 X 95, LEFT EYE PRE-OP 20/20 -.50 X -.50 X 75. THIS REPORT IS FOR THE EXCIMER LASER. A SEPARATE REPORT WILL BE SUBMITTED FOR THE FEMTO LASER.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 213426 | STAR | EXCIMER LASER | LZS | JOHNSON & JOHNSON SURGICAL VISION, INC | 0030-2450 | 00(01)(21)5330 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 36 YR | Required Intervention | FEMTO LASER SERIAL NO. (B)(4) |