inforMED
MalfunctionOOE

WAVELIGHT FS200 FEMTOSECOND LASER

Received Jun 17, 2026

Report 3003288808-2026-00279 · MDR key 25529867

Device

Generic name

Ophthalmic Laser

Manufacturer

Wavelight Gmbh

Model number

NA

Catalog number

8065000123

Lot number

14UPFA

Product problems

  • Unexpected Therapeutic Results

Patient

38 YR · Female

  • Insufficient Information

Narrative

Description of Event or Problem

A PHYSICIAN REPORTED THAT DOCTOR NOTICED NO SIDE CUT IN THE RIGHT EYE OF THE PATIENT DURING REFRACTIVE SURGERY AND DECIDED TO ALLOW THE EYE TO HEAL FOR RETREATMENT AGAIN IN FEW WEEKS. THE PROCEDURE WAS NOT COMPLETED. THERE ARE TWO RELATED REPORTS FOR THIS PATIENT. THIS REPORT ADDRESSES THE PATIENT'S RIGHT EYE AND ANOTHER MANUFACTURER REPORT WILL BE FILED FOR THE FELLOW EYE.

Additional Manufacturer Narrative

H.3., H.6.: INVESTIGATION, INCLUDING ROOT CAUSE ANALYSIS, IS IN PROGRESS. A SUPPLEMENTAL MDR WILL BE FILED AS NECESSARY IN ACCORDANCE WITH 21 CFR 803.56 WHEN ADDITIONAL REPORTABLE INFORMATION BECOMES AVAILABLE. THE MANUFACTURER INTERNAL REFERENCE NUMBER IS: (B)(4).