FDA Recall D-0409-2026
K.C. Pharmaceuticals, Inc · Pomona, CA
Class II Ongoing 72 days on record
Product
Sterile EYE DROPS AC (tetrahydrozoline HCl 0.05%, zinc sulfate 0.25%), 0.5 fl. oz. (15 mL) bottles; a) Best Choice, PROUDLY DISTRIBUTED BY: VALU MERCHANDISERS, CO., 5000 KANSAS AVE, KANSAS CITY, KS 66106, UPC 0 70038 47010 6; b) QC-Quality Choice, Sterile Eye drops Irritation Relief, Distributed by: CDMA, Inc., Novi, MI 48375, NDC 83324-190-14; c) Discount drug mart, Eye Drops A.C., Discount Drug Mart Food Fair, Medina, OH 44256, UPC 0 93351 01158 0; d) Good Sense Sterile Eye Drops, Distributed By: Perrigo Direct, Inc., Peachtree City, GA 30269, www.PerrigoDirect.com, NDC 50804-160-01; e) Walgreens, Eye Drops, DISTRIBUTED BY: WALGREEN CO., DEERFIELD, IL 60015, UPC 3 11917 17954 4; f) CAREONE, Itchy relief Eye drops, DISTRIBUTED BY: FOODHOLD U.S.A, LLC., LANDOVER, MD 20785; g) Equaline, DISTRIBUTED BY: UNFI, PROVIDENCE, RI 02908 UPC 0 41163 25114 4; h) TopCare health TM, DISTRIBUTED BY: TOPCO ASSOCIATES LLC, ELK GROVE VILLAGE, IL 60007, UPC 0 36800 03640 6; i) meijer, DIST. BY MEIJER DISTRIBUTION, INC., GRAND RAPIDS, MI 49544, www.meijer.com, NDC 41250-598-01; j) H.E.B A.C. Eye Drops, MADE WITH PRIDE & CARE FOR H-E-B, SAN ANTONIO, TX 78204, UPC 0 41220 43746 7
Reason for recall
Lack of Assurance of Sterility
Recall record
- Recall number
D-0409-2026- Classification
- Class II
- Status
- Ongoing
- Voluntary or mandated
- Voluntary: Firm initiated
- Firm notification
- Distribution
- Nationwide in the US
- Recall initiated
- 2026-03-03
- Classified by FDA Center
- 2026-03-31
- FDA published
- 2026-04-08
- Recalling firm
- K.C. Pharmaceuticals, Inc
- Firm location
- Pomona, CA
Drug identification
- Brand name(s)
- QUALITY CHOICE EYE DROPS IRRITATION RELIEF, GOODSENSE ULTRA LUBRICANT EYE DROPS, MEIJER SEASONAL ITCHING AND REDNESS RELIEF
- Generic name(s)
- TETRAHYDROZOLINE HCL, ZINC SULFATE, POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL, TETRAHYDROZOLINE HCI, ZINC SULFATE
- Manufacturer(s)
- Quality Choice, Geiss, Destin & Dunn, Inc., Meijer Distribution, Inc.
- NDC(s)
83324-190, 50804-160, 41250-598- Route(s)
- OPHTHALMIC
Operational response
Class II recalls indicate possible temporary or reversible health consequences. Remove affected lots from active dispensing. Segregate inventory. Check the firm’s recall notification for guidance on patient outreach.
For the official FDA enforcement record, see FDA's Recall Search.