Clear Care Clear Care 2x12oz (UDI 00047113609027)Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00047113609027), received between Oct 8, 2020 and Jul 23, 2025 — classified as 4 injuries.

The most frequently reported specific device problem is “Improper Chemical Reaction” (1 report).

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 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• InjuryJul 23, 2025Improper Chemical Reaction; Improper Chemical Reaction

  AS INITIALLY THE REPORTED BY THE CONSUMER STATING THAT THE CONSUMER EXPERIENCED SERIOUS EYE INJURY CAUSED BY THE CONTACT LENS SOLUTION EVEN AFTER FOLLOWING ALL INSTRUCTION AND NEUTRALIZING. THE CUSTOMER SUFFERED A CHEMICAL BURN TO THE EYE, WHICH LED TO A RUPTURED AND ONE MM MARGINAL CORNEAL ULCER IN THE LEFT EYE. THE INJURY REQUIRED MULTIPLE DOCTOR VISITS, PRESCRIPTIONS FOR ANTIBIOTIC AND STEROID EYE DROPS, AND WEEKS WITHOUT BEING ABLE TO WEAR CONTACT LENSES. CUSTOMER HAD TO WEAR GLASSES, WHICH IMPACTED THE VISION. THE CONTACT LENS CARE SUDDENLY STOPPED NEUTRALIZING PROPERLY WHICH RESULTED IN VISION PROBLEM IN ONE EYE. THE INJURY HAD RESULTED IN BLURRY VISION IN THE AFFECTED EYE ALONG WITH DISCOMFORT EVENT AFTER MEDICAL TREATMENT. DURING FOLLOW UP IT WAS ALSO DIAGNOSED TO HAVE CORNEAL KERATITIS. THE CURRENT STATUS OF THE CONSUMER'S EYE IS SYMPTOM RESOLVED AND THE CUSTOMER HAS RESUMED CONTACT LENS WEAR. NO ADDITIONAL INFORMATION HAS BEEN REQUESTED.

  Patient problems: Blurred Vision; Corneal Ulcer; Discomfort; Eye Burn; Eye Irritation; Eye Pain; Keratitis; Photophobia; Red Eye(s)

  MAUDE report 22573552 ↗
• InjuryOct 28, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  AS INITIALLY REPORTED FROM ATTORNEY TO LEGAL TEAM ON BEHALF OF THE CONSUMER STATING THAT CONSUMER EXPERIENCED FOREIGN BODY SENSATION, BLURRED VISION, PAIN, PHOTOPHOBIA, AND RED EYE, WHICH WERE SEVERE IN NATURE IN RELATION TO THE RIGHT EYE (OD) FOR DURATION OF THREE WEEKS. CONSUMER SOUGHT MEDICAL ATTENTION FOR THE ABOVE SYMPTOMS. ON SLIT EXAMINATION OD HAD FOLLOWING FINDINGS GRANULAR KERATITIS (POORLY DEFINED WHITENING/ GREYING, NO WELL-DEFINED INFILTRATE) (1.2MM(V) X 2.0(H)) EPITHELIAL DEFECT. DIFFERENTIAL DIAGNOSIS OF HERPES SIMPLEX VIRUS, BACTERIAL, FUNGAL AND ACANTHAMOEBA WAS CONSIDERED. ADVISED FOR CORNEAL CULTURE AND CORNEAL PCR (POLYMERASE CHAIN REACTION) TESTS . DIAGNOSIS OF CENTRAL CORNEAL ULCER OF OD WAS PROVIDED FROM THE EYE CARE PROFESSIONAL (ECP).SHE WAS PRESCRIBED WITH MOXIFLOXACIN 0.5 % EYE DROPS, TO BE APPLIED ONE DROP IN THE RIGHT EYE EVERY TWO HOURS TILL NEXT VISIT, ERYTHROMYCIN 5 MG/GRAM (0.5 %) EYE OINTMENT, TO BE ADMINISTERED PEA-SIZED AMOUNT INTO RIGHT EYE THREE TIMES DAILY TILL NEXT VISIT., VALACYCLOVIR TABLET;1 GRAM, TO BE TAKEN ORALLY THREE TIMES DAILY TILL NEXT VISIT AND ADVISED FOR FOLLOW UP AFTER TWO DAYS FOR FURTHER EVALUATION AND MANAGEMENT . CONSUMER W

  Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available; Blurred Vision; Corneal Abrasion; Corneal Infiltrates; Corneal Ulcer; Erosion; Eye Irritation; Eye Pain; Infective Keratitis; Iritis; Photophobia; Ptosis; Purulent Discharge; Red Eye(s)

  MAUDE report 20542404 ↗
• InjuryApr 13, 2023Use of Device Problem; Use of Device Problem

  NON-HEALTH CARE PROFESSIONAL REPORTED ON BEHALF OF A CONSUMER, WHO EXPERIENCED SEVERE DAMAGE TO THE PUPIL, LOSS OF VISION IN LEFT EYE AND SIGNIFICANT DISTRESS AFTER USING CLEANING AND DISINFECTING SOLUTION. THE CONSUMER USED THE EXPIRED PRODUCTS. THE CURRENT STATUS OF THE CONSUMER'S EYE IS NOT RESOLVED AT THE TIME OF THIS REPORT. ADDITIONAL INFORMATION HAS BEEN REQUESTED BUT NOT YET RECEIVED.

  Patient problems: Corneal Abrasion; Distress; Loss of Vision

  MAUDE report 16730075 ↗
• InjuryOct 8, 2020Patient-Device Incompatibility

  CONSUMER CALLED TO REPORT THAT AFTER USING CLEAR CARE 3% HYDROGEN PEROXIDE CLEAN AND DISINFECTANT SOLUTION (OPHTHALMIC SOLUTION), SHE EXPERIENCED SEVERE EYE BURNING AND WATERY EYES. CONSUMER BELIEVES THAT THE DISC THAT IS SUPPOSED TO BE AT THE BOTTOM OF THE SOLUTION BOTTLE, DOES NOT LAST FOR THE DURATION OF THE PRODUCT, SO THE SOLUTION NO LONGER IS BEING NEUTRALIZED. CONSUMER HAS CONTACTED THE MANUFACTURER VIA EMAIL, AND HAS YET TO RECEIVE A RESPONSE. SHE HAS AUTHORIZED FDA TO PROVIDE HER NAME IN ORDER TO FACILITATE THE COMPLAINT FOLLOW-UP. EYE IRRITATION.

  Patient problems: Burning Sensation; Excessive Tear Production; Irritation

  MAUDE report 10658443 ↗