CLASS II ONGOING Drug recall · Reported 14 Oct 2026 · FDA Enforcement Report

Sterile EYE Drops AC (tetrahydrozoline HCl recalled

K.C. Pharmaceuticals is recalling Sterile EYE Drops AC (tetrahydrozoline HCl 0.05%, zinc sulfate 0.25%), distributed nationwide in the US. The recall was initiated on 11 Sep 2026 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot: a) AC25C01, Exp.: 3/31/2027; b) AC25B01, Exp.: 2/28/2027; AC25C01, Exp.: 3/31/2027; c) AC25C01, Exp.: 3/31/2027; d) AC25C01, Exp.: 3/31/2027; e) AC25C01, Exp.: 3/31/2027.
NDC50804-121, 83324-190
UPC0180410000187, 0635515995055, 041163251144, 041220437467, 036800036406
Quantity recalled182,016 cartons

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

Recall details

Recall number
D-0003-2027
FDA event ID
99880
Recalling firm
K.C. Pharmaceuticals, Pomona, CA
Manufacturer
Geiss, Destin & Dunn, Inc.
Classification
Class II
Status
Ongoing
Recall initiated
11 Sep 2026
FDA classified
5 Oct 2026
Reported
14 Oct 2026
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Sterility
Drug class
Eye Drops

Timeline

11 Sep 2026Recall initiated by company
5 Oct 2026Classified by FDA+24 days
14 Oct 2026Published in enforcement report+9 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Lack of Assurance of Sterility

A sterility recall means a product that must be sterile, such as an injection or eye drop, may be contaminated. Using a non-sterile product can cause serious infection.

Product as listed by the FDA

Sterile EYE DROPS AC (tetrahydrozoline HCl 0.05%, zinc sulfate 0.25%), 0.5 fl. oz. (15 mL) bottles; a) Equaline, DISTRIBUTED BY: UNFI, PROVIDENCE, RI 02908 UPC 0 41163 25114 4; b) Good Sense Sterile Eye Drops, Distributed By: Geiss, Destin & Dunn, Inc., A Perrigo Company, Peachtree City, GA 30269, NDC 50804-121-01; c) H.E.B A.C. Eye Drops, MADE WITH PRIDE & CARE FOR H-E-B, SAN ANTONIO, TX 78204, UPC 0 41220 43746 7; d) QC-Quality Choice, Sterile Eye drops Irritation Relief, Distributed by: CDMA, Inc., Novi, MI 48375, NDC 83324-190-14; e) TopCare health TM, DISTRIBUTED BY: TOPCO ASSOCIATES LLC, ELK GROVE VILLAGE, IL 60007, UPC 0 36800 03640 6.

Where it was distributed

US Nationwide

Nationwide

Stores named: H-E-B

Questions about this recall

Why was it recalled?

Lack of Assurance of Sterility

Which lots are affected?

Lot: a) AC25C01, Exp.: 3/31/2027; b) AC25B01, Exp.: 2/28/2027; AC25C01, Exp.: 3/31/2027; c) AC25C01, Exp.: 3/31/2027; d) AC25C01, Exp.: 3/31/2027; e) AC25C01, Exp.: 3/31/2027.

Where was it sold?

US Nationwide

What should I do if I have it?

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 Oct 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

7 other products · FDA event 99880

This product is part of a recall event; the main page for the event is Sterile Lubricant Dry Eye Relief Eye Drops recalled.

ReportedClassRecallCompanyReasonWhere
CLASS IISterile Lubricant Dry Eye Relief Eye Drops recalledLeader Dry Eye Relief Eye DropsK.C. PharmaceuticalsSterilityNationwide
CLASS IISterile EYE Drops Advanced Relief, (dextran recalledLeader Advanced Relief Eye DropsK.C. PharmaceuticalsSterilityNationwide
CLASS IISterile Eye Drops, Original recalled by K.C. PharmaceuticalsGoodsense Eye Drops Original FormulaK.C. PharmaceuticalsSterilityNationwide
CLASS IISterile High Performance Ultra Lubricating Eye Drops recalledLeader Ultra Lubricating Eye DropsK.C. PharmaceuticalsSterilityNationwide
CLASS IIEye Drops Maximum, Redness Relief, Sterile recalledTarget Eye Drops Maximum Redness Relief EyeK.C. PharmaceuticalsSterilityNationwide
CLASS IIArtificial Tears Sterile Lubricant Eye Drops recalledLeader Artificial Tears 15 MlK.C. PharmaceuticalsSterilityNationwide
CLASS IISterile Eye Drops Redness Relief (Glycerin recalledLeader Eye Drops Redness ReliefK.C. PharmaceuticalsSterilityNationwide

More recalls from K.C. Pharmaceuticals

All 23
ReportedClassRecallCompanyReasonWhere
DrugCLASS IISterile Eye Drops Redness Relief (Glycerin recalledLeader Eye Drops Redness ReliefK.C. PharmaceuticalsSterilityNationwide
DrugCLASS IIArtificial Tears Sterile Lubricant Eye Drops recalledLeader Artificial Tears 15 MlK.C. PharmaceuticalsSterilityNationwide
DrugCLASS IIEye Drops Maximum, Redness Relief, Sterile recalledTarget Eye Drops Maximum Redness Relief EyeK.C. PharmaceuticalsSterilityNationwide
DrugCLASS IISterile High Performance Ultra Lubricating Eye Drops recalledLeader Ultra Lubricating Eye DropsK.C. PharmaceuticalsSterilityNationwide
DrugCLASS IISterile Eye Drops, Original recalled by K.C. PharmaceuticalsGoodsense Eye Drops Original FormulaK.C. PharmaceuticalsSterilityNationwide

Other Tetrahydrozoline recalls

All 7
ReportedClassRecallCompanyReasonWhere
DrugCLASS IISterile Eye Drops, Original recalled by K.C. PharmaceuticalsGoodsense Eye Drops Original FormulaK.C. PharmaceuticalsSterilityNationwide
DrugCLASS IISterile EYE Drops AC (tetrahydrozoline HCl recalledQuality Choice Eye Drops Irritation ReliefK.C. PharmaceuticalsSterilityNationwide
DrugCLASS IISterile Eye Drops Original Formula (tetrahydrozoline HCl 0.05%) recalledGoodsense Eye Drops Original FormulaK.C. PharmaceuticalsSterilityNationwide
DrugCLASS IIOriginal Eye Drops recalled by K.C. PharmaceuticalsSunmark Eye Drops Original FormulaK.C. PharmaceuticalsManufacturing (CGMP) DeviationsNationwide
DrugCLASS IIIEye Drops (Tetrahydrozoline HCl 0.05%), Over the Counter recalledSunmark Eye Drops Original FormulaK C PharmaceuticalsManufacturing (CGMP) DeviationsNationwide