Over 500,000 eye drop products have been recalled over sterility concerns. As reported by People, the recall has been designated a Class II by the FDA.
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Which Eye Drops Have Been Recalled?
Nine separate types of products have been recalled in all. Here's a full list:
| Product | Recall Number | Code Information | Product Quantity |
|---|---|---|---|
| AvKare Lubricant Eye Drops | D-0855-2026 | Lots 3161, 3245, 3260, 3298-3302, 3305-3306; Exp. 8/2026-7/2027 | 12,864 packs |
| Reliable-1 Sodium Chloride Eye Solution | D-0856-2026 | Lots 3192, 3293, 3336; Exp. 1/31/2027-6/30/2027 | 11,083 bottles |
| Walgreens Lubricant Eye Drops | D-0857-2026 | Lots 3166, 3172, and others | 301,114 bottles |
| Walgreens Lubricant Eye Drops Twin Pack | D-0858-2026 | Lots 3165, 3179, 3204, 3206, 3208, 3259, 3265, 3268, and others | 199,600 packs |
| Reliable-1 Lubricating Tears | D-0859-2026 | Lots 3171, 3174, 3275, 3304; Exp. 9/30/2026-7/31/2027 | 47,616 bottles |
| TRP Gentle Eyes Lubricant Eye Drops | D-0860-2026 | Lots 3279, 3292; Exp. 5/31/2027-6/30/2027 | 14,538 bottles |
| Major LubriFresh P.M. Nighttime Ointment | D-0861-2026 | Lot 3183 | 34,368 tubes |
| Cameron Pharmaceuticals Lubricant Eye Drops | D-0862-2026 | Lots 3163, 3164; Exp. 8/31/2026-9/30/2026 | 19,284 bottles |
| AvKare Lubricant Eye Drops Twin Pack | D-0863-2026 | Lots 3161, 3245, 3260, 3298-3302, 3305-3306; Exp. 8/2026-7/2027 | 107,377 packs |
The affected eye drops were distributed by Sterling Pharmaceutical Services LLA, which is based in Dupo, Illinois. The affected products were sold in a number of locations under several brand names, including Walgreens.
What is Wrong With the Product?
The company issued a voluntary recall following concerns about a lack of sterility: the FDA has classified this recall as a Class II.
A Class II recall occurs when the "use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote."
What Should I Do if My Product Is Affected?
The FDA has advised that, if you believe your product is affected, the first thing you should do is stop using it immediately.
Concerned customers should then contact their healthcare provider in order to find out their next steps.
Luckily, no one has reported any injuries or other health concerns from the use of the eye drops—here's hoping that stays the case.
