OPTI-FREE PUREMOIST OPTI-FREE PUREMOIST 2x10ozRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00300650361057), received between Jan 12, 2026 and Jan 12, 2026 — classified as 1 injury.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjuryJan 12, 2026Adverse Event Without Identified Device or Use Problem

  AS INITIALLY REPORTED BY CONSUMER STATING THAT THE CONSUMER STARTED EXPERIENCED BURNING, EYE PAIN APPROXIMATELY TWO WEEKS BEFORE CONSUMER WENT TO PRIMARY CARE PROVIDER AS WELL AS EYE DOCTOR, AT FIRST, THEY THOUGHT THAT IT WAS DUE TO CONTACT LENS, AS IT WAS APPROACHING THE ONE-MONTH TIME FRAME AND USED NEW CONTACTS WITH NO IMPROVEMENT. THE INFECTION WAS SO SEVERE THAT THE CONSUMER HAD EXTREME LIGHT SENSITIVITY AND MIGRAINES. THE CONSUMER SOUGHT MEDICAL INTERVENTION AND DIAGNOSED WITH KERATITIS. THE CONSUMER WAS PRESCRIBED WITH UNSPECIFIED STEROID EYE DROPS. THE CURRENT STATUS OF THE CONSUMER¿S EYE WAS SYMPTOMS IMPROVING AT THE TIME OF THIS REPORT. ADDITIONAL INFORMATION HAS BEEN REQUESTED BUT NOT YET RECEIVED. ADDITIONAL INFORMATION RECEIVED STATING THAT CONSUMER ALSO EXPERIENCED RED EYE, TWO WEEKS AFTER DOCTOR VISIT AND TREATMENT WITH STEROID EYE DROP THE CONSUMER TRIED TO WEAR A BRAND-NEW PAIR OF CONTACTS WHICH WENT WELL THE FIRST DAY, HOWEVER AFTER SOAKING OVERNIGHT IN THE SOLUTION THE CONSUMER'S EYE WAS IRRITATED. THE CONSUMER STOPPED USING THE SOLUTION. AFTER CHANGING THE SOLUTION, THE CONSUMER WAS ABLE TO WEAR CONTACTS BUT NOT FOR A FULL DAY AS BEFORE. THE CURRENT STATUS OF TH

  Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available; Burning Sensation; Eye Irritation; Eye Pain; Keratitis; Photophobia; Red Eye(s)

  MAUDE report 24034053 ↗