Recalls / Class II
Class IID-0410-2026
Product
EYE DROPS Advanced Relief, (dextran 70 0.1%, polyethylene glycol 400 1% and tetrahydrozoline HCl 0.05%), 0.5 FL OZ (15 mL) bottles, Sterile; a) Walgreens, DISTRIBUTED BY: WALGREEN CO., DEERFIELD, IL 60015; UPC 3 11917 20074 3; b) Kroger, DISTRIBUTED BY THE KROGER CO., CINCINNATI, OHIO 45202; c) CVS Health, Distributed by :CVS Pharmacy, Inc., Woonsocket, RI 02895, UPC 0 50428 43544 1; d) QC-Quality Choice, Distributed by: CDMA, Inc., Novi, MI 48375, NDC 83324-191-14; e) Discount drug mart, Discount Drug Mart Food Fair, Medina, OH 44256, UPC 0 93351 01155 9; f) Foster & Thrive, Distributed by: McKesson Corp., via SSSL, Memphis, TN 38141, NDC 70677-1158-1; g) GoodSense, Distributed By: Perrigo Direct Inc., Peachtree City, GA 30269, www.PerrigoDirect.com, NDC 50804-130-01; h) TopCare health, DISTRIBUTED BY TOPCO ASSOCIATES LLC, ELKGROVE VILLAGE, IL 60007, UPC 0 36800 03641 3; I) DG health Sterile, DISTRIBUTED BY OLD EAST MAIN CO., 100 MISSION RIDGE, GOODLETTSVILLE, TN 37072, UPC 0 95072 02556 3; j) Fast Acting, CODE RED Eye Drops, Sterile, Distributed by: 4 Trees, LLC, NDC 83817-963-01.
- Brand names
- Quality Choice Moisturizing Relief Eye Drops, Foster And Thrive Advanced Relief Eye Drops, Goodsense Eye Drops Advanced Relief Moisturizer, Code Red Eye Drops Redness Relief
- Generic names
- Dextran 70, Polyethylene Glycol 400, Povidone, Tetrahydrozoline Hcl, Polyethylene Glycol 400, Tetrahydrozoline Hcl, Dextran, Polyethylene Glycol 400, Povidone, Tetrahydrozoline Hcl
- Active ingredients
- Dextran 70, Polyethylene Glycol 400, Povidone, Tetrahydrozoline Hydrochloride
- Route
- Ophthalmic
- NDCs
- 83324-191, 70677-1158, 50804-130, 83817-963
- FDA application
- M018
- Affected lot / code info
- Lot: a) AR24D01, Exp.: 04/30/26; AR24G01, AR24G02, Exp.: 07/31/26; AR24M01, Exp.: 10/31/26; b) AR24D01, Exp.: 04/30/26; AR24G01, Exp.: 07/31/26; AR24M01, Exp.: 10/31/26; c) AR24D01, Exp.: 04/30/26; AR24G02, Exp.: 07/31/26; AR24M01, Exp.: 10/31/26; d) AR24G02, Exp.: 07/31/26; e) AR24G02, Exp.: 07/31/26; f) AR24G02, Exp.: 07/31/26; g) AR24M01, Exp.: 10/31/26, h) AR24G01, Exp.: 07/31/26; AR24M01, Exp.:10/31/26; I) AR24M01, Exp.:10/31/26; j) AR24D01, Exp.: 04/30/26.
Why it was recalled
Lack of Assurance of Sterility
Recalling firm
- Firm
- K.C. Pharmaceuticals, Inc
- Manufacturer
- Chain Drug Marketing Association, Inc.
- Notification channel
- Type
- Voluntary: Firm initiated
- Address
- 3420 Pomona Blvd, Pomona, California 91768-3236
Distribution
- Quantity
- 303,216 bottles
- Distribution pattern
- Nationwide in the US
Timeline
- Recall initiated
- 2026-03-03
- FDA classified
- 2026-03-31
- Posted by FDA
- 2026-04-08
- Status
- Ongoing
Source: openFDA Drug Enforcement endpoint. Recall record D-0410-2026. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.