More than 1.02 million bottles of Dry Eye Relief Eye Drops across multiple brands were recalled nationwide on March 3, 2026. The products were distributed by KC Pharmaceuticals and sold at retailers including Rite Aid, Meijer and H-E-B. The FDA notice cites a lack of assurance of sterility as the reason for the recall. Stop using these products immediately and contact KC Pharmaceuticals for next‑s
Lack of Assurance of Sterility
Consumers and healthcare providers should stop using this product immediately. Contact K.C. Pharmaceuticals, Inc or your healthcare provider for guidance. Notification method: E-Mail
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Dry Eye Relief Eye Drops are marketed as artificial tears to lubricate the eye. The recall encompasses multiple brand names and distributors with nationwide distribution.
A lack of sterility can lead to eye infections or other ocular harm; users should avoid continued use and seek guidance from a clinician.
This recall is not described as part of a broader industry pattern in the provided notice.
Consumers face potential eye infections when using sterile-sensitive ophthalmic products. The recall involves a large quantity and widespread retailers, necessitating prompt action.
Official recall information is available on the FDA enforcement notice linked in the recall summary. Additional details may be on retailer recall notices.
Refunds or replacements, if offered, typically take 4-6 weeks after a claim is submitted.
Keep the recall notice, bottle packaging, lot numbers, and all correspondence with the company and healthcare providers for records.
1,023,096 bottles recalled nationwide. Distributed by KC Pharmaceuticals, Inc. and sold under multiple brand names (ARTIFICIAL TEARS, RITE AID EYE DROPS DRY EYE RELIEF, LEADER DRY EYE RELIEF EYE DROPS, FOSTER AND THRIVE ADVANCED RELIEF EYE DROPS, MEIJER DRY EYE RELIEF, and others). 0.5 FL OZ (15 mL) bottles. NDCs and UPCs vary by brand. The recall covers lots LT24E01, LT24E02, LT24E03, LT24F01, LT24G01, LT24M01, LT24M02 with expirations through 2026 (05/31/26 to 10/31/26). Nationwide distribution in the United States.
No injuries or incidents have been reported.
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