RecallReported October 14, 2026
Class II recall by K.C. Pharmaceuticals, Inc.
Sterile Lubricant Dry Eye Relief Eye Drops, 0.5 FL OZ (15 mL); a) LEADER, DISTRIBUTED BY CARDINAL HEALTH, DUBLIN, OHIO 43017, www.myleader.c…
FDA's enforcement report of October 14, 2026 lists a Class II recall by K.C. Pharmaceuticals, Inc. of Pomona, CA. Product: Sterile Lubricant Dry Eye Relief Eye Drops, 0.5 FL OZ (15 mL); a) LEADER, DISTRIBUTED BY CARDINAL HEALTH, DUBLIN, OHIO 43017, www.myleader.c…. Status: Ongoing.
On the record
- Recalling firm
- K.C. Pharmaceuticals, Inc.
- Location
- Pomona, CA
- Classification
- Class II
- Status
- Ongoing
- Recall number
- D-0006-2027
- Product type
- Drugs
- Brand names
- LEADER DRY EYE RELIEF EYE DROPS, ARTIFICIAL TEARS, FOSTER AND THRIVE DRY EYE RELIEF
- Generic names
- GLYCERIN, HYPROMELLOSE, POLYETHYLENE GLYCOL 400, GLYCERIN, POLYETHYLENE GLYCOL 400
- Recall initiated
- 2026-09-11
- Reported by FDA
- 2026-10-14
The full record
An account shows the reason for the recall, where the product was distributed and the lots.
What a recall is
FDA classifies a recall by the hazard. Class I: a reasonable probability that the product will cause serious adverse health consequences or death. Class II: the product may cause temporary or medically reversible harm, or the probability of serious harm is remote. Class III: the product is not likely to cause adverse health consequences.
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From FDA enforcement reports. The record may have changed since it was read.
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