Rexall 68090DGRecalls & reported problems
Apothecary Products, LLC · DG OPP CONTACT CASE 1CT · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00023185002003), received between Sep 24, 2021 and Sep 24, 2021 — classified as 1 injury.
The most frequently reported specific device problem is “Use of Device 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. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Use of Device Problem1
Patient problems
- Insufficient Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjurySep 24, 2021Use of Device Problem; Use of Device Problem
CUSTOMER PURCHASED CONTACT LENS CASE ON WED NIGHT (B)(6) 2021 FROM THE (B)(6) STORE. WASHED HANDS AND FACE AND TOOK CONTACT LENSES OUT AND PUT SOLUTION IN AND PUT CONTACT LENSES IN THE CASE. NEXT MORNING, PUT CONTACT LENSES IN, RIGHT EYE FIRST AND THEN LEFT EYE. SHE IMMEDIATELY EXPERIENCED PAIN IN THE LEFT EYE. SHE ORIGINALLY THOUGHT CONTACT LENS HAD FOLDED BUT THERE WAS SOMETHING ELSE BEHIND THE LENS. TOOK 20 MINUTES TO GET CONTACT OUT. NORMALLY TAKES 2 SECONDS TO PULL IT OUT. COULDN'T GET EYE OPEN. WATERING FROM IRRITATION. FINALLY GOT LENS OUT, HELD EYE OPEN AND TRIED TO GET THE PIECE OF PLASTIC OUT THAT WAS CURVED LIKE AN EYELASH. COULDN'T GET IT OUT. HUSBAND TOOK HER TO URGENT CARE. THEY TOOK HER BACK IMMEDIATELY AND PUT HER EYE UNDER A FAUCET FOR 5 MINUTES TO FLUSH IT OUT. WHEN IT CAME OUT, THEY DRIED HER EYE AND THEY PUT IN SOME PAIN-RELIEVING DROPS THAT NUMBED HER EYE. PUT DYE IN EYE AND LOOKED UNDER A BLACK LIGHT AND DETERMINED THERE WAS A LACERATION ON HER CORNEA. HAD TO PRESCRIBE AN ANTIBIOTIC OINTMENT. STARTED USING OINTMENT IMMEDIATELY AND THE OINTMENT WAS KIND OF GRITTY WHICH WAS REALLY PAINFUL. THEN SHE CALLED A TELEHEALTH PERSON TO SEE IF SHE COULD GET A PAIN-RELIEV
Patient problems: Insufficient Information
MAUDE report 12530246 ↗
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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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