BLINK CONTACTS 90222HZRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00827444000324), received between Jan 27, 2017 and Jun 22, 2017 — classified as 1 injury, 1 malfunction.

The most frequently reported specific device problem is “Device Markings/Labelling Problem” (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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryJun 22, 2017Shelf Life Exceeded; Shelf Life Exceeded

  IT WAS REPORTED THAT THE PATIENT STARTED EXPERIENCING SWOLLEN EYELIDS FOLLOWING USE OF BLINK CONTACTS. PATIENT CONTINUED TO USE HER BOTTLE OF BLINK CONTACTS BECAUSE SHE IS JUST NOW STARTING TO CONNECT THE SWELLING WITH IT. SHE OPENED THE BOTTLE IN EARLY (B)(6) AND HAS BEEN USING IT FOR LONGER THAN 45 DAYS, WHICH IS BEING NOTED AS MISUSE OF THE PRODUCT. HER EYELIDS HAVE BEEN AN ISSUE SINCE (B)(6). PATIENT SAID SHE HAS USED BLINK CONTACTS FOR APPROXIMATELY 10 YEARS WITHOUT ANY ISSUES. WHEN SHE WENT TO HER DOCTOR HE GAVE HER AN ANTIBIOTIC OINTMENT- NEOMYCIN USING IT 2X DAY, MORNING AND NIGHT. THAT DID NOT RESOLVE IT, SO THEN HE GAVE HER ANOTHER ANTIBIOTIC OINTMENT - TOPAREX TO USE 2X DAY. DOCTOR TOLD HER IT'S AN ALLERGIC SENSITIVITY TO SOMETHING SHE IS USING. PATIENT WAS INFORMED TO DISCONTINUE USE OF HER BOTTLE.

  Patient problems: No Code Available

  MAUDE report 6662003 ↗
• MalfunctionJan 27, 2017Device Markings/Labelling Problem; Device Markings/Labelling Problem

  IT WAS REPORTED THAT A CUSTOMER PURCHASED BLINK CONTACTS AND THE BOTTLE WAS PLAIN GREEN WITH NO LABELING ON IT. THE BOX WAS SEALED AT TIME OF PURCHASE AND HAD LOT NUMBER AND EXPIRATION DATE. THE CUSTOMER REPORTED THAT HE HAD USED THE PRODUCT AND DID NOT HAVE ANY ISSUES. THE PRODUCT WAS RETURNED.

  Patient problems: No Patient Involvement

  MAUDE report 6284496 ↗