BLINK-N-CLEAN 93945HZRecalls & reported problems
Bausch & Lomb Incorporated · BLINK-N-CLEAN 15 ML · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00827444000126), received between Jan 27, 2017 and Jan 24, 2020 — classified as 2 injuries.
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
Device problems
- Adverse Event Without Identified Device or Use Problem2
Patient problems
- Dry Eye(s)2
- Discomfort1
- Headache1
- Irritation1
- Pain1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryJan 24, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
CONSUMER REPORTED THAT SHE PURCHASED BLINK AND CLEAN LENS DROPS AROUND (B)(6) BUT UPON USING THE DROPS SHE EXPERIENCED IRRITATION, TINGLING AND BUMPS. SHE STOPPED USING THE DROPS AND THE SYMPTOMS ABATED. HER DOCTOR PRESCRIBED ANTIBIOTICS AND BLINK LUBRICATING DROPS FOR HER DRY EYE AND TO PROVIDE IMMEDIATE COMFORT. SHE TRIED THE BLINK AND CLEAN LENS DROPS AGAIN YESTERDAY ((B)(6) 2020) AND EXPERIENCED THE SAME THING PLUS IRRITATION ON THE EYE LID AND THE SKIN AROUND THE EYE. HER EYES FEEL BETTER BUT ARE STILL TENDER. THRU ADDITIONAL FOLLOW-UP THE CONSUMER REITERATED THAT HER EYES FEEL BETTER ALTHOUGH THERE IS STILL DISCOMFORT. ADDITIONALLY, SHE REPORTED THAT HER EYES ARE SENSITIVE TO ¿SCREENS¿ AND LIGHT. NO FURTHER INFORMATION WAS PROVIDED.
Patient problems: Discomfort; Dry Eye(s); Irritation
MAUDE report 9628992 ↗InjuryJan 27, 2017Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
A FEMALE PATIENT REPORTED THAT SHE USED BLINK-N-CLEAN LAST NIGHT FOR THE FIRST TIME. SHE PUT 2 DROPS IN HER RIGHT EYE AND IMMEDIATELY IT STARTED BURNING AND SHE COULD FEEL PAIN. WHEN SHE LOOKED AT HER EYE IN THE MIRROR, SHE COULD SEE BLISTERS THAT LOOKED LIKE RAISED RED DOTS AND ALSO EXPERIENCED BLURRING. PATIENT WENT TO THE EMERGENCY ROOM AND THE DOCTOR TOLD HER THAT HE HAD NEVER SEEN ANYTHING LIKE IT. IT LOOKED LIKE SHE GOT HIT WITH A FLASH OF INDUSTRIAL CLEANER. DOCTOR FLUSHED HER EYE OUT FOR APPROXIMATELY 3 MINUTES AND HER CONTACT CAME OUT. CONTACT LOOKED ALMOST MELTED, IT LOST ITS SHAPE. PATIENT USES COLORED CONTACTS FOR APPEARANCE, NOT VISION. DOCTOR ALSO GAVE PATIENT A PAIN SHOT (10 MGS. OF DILAUDID). DOCTOR RECOMMENDED AN EYE DROP NAMED, ROHTO ICE TO MOISTURIZE. THE NEXT DAY SHE WENT TO SEE AN OPTOMETRIST, AND WAS TOLD IT DOES LOOK LIKE AN INDUSTRIAL ACID BURN. DOCTOR GAVE THE PATIENT A PRESCRIPTION FOR RESTASIS TO USE FOR SEVEN MORE DAYS. DOCTOR TOLD PATIENT THAT IF HER EYE DOESN'T FEEL BETTER, COME BACK IN IMMEDIATELY. PATIENT WAS ALSO TOLD THAT HER EYE SHOULD HEAL ON ITS OWN AND NOT TO WEAR HER CONTACTS. DOCTOR DID PUT A DROP IN HER EYE, BUT SHE DOESN'T KNOW THE NAME OF
Patient problems: Dry Eye(s); Headache; Pain
MAUDE report 6284883 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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