US Drug Recall Register
Class II · Moderate risk Ongoing Initiated May 28, 2026 (3 months ago)

GOODSENSE Ultra Strength

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Presence of foreign substance: small metallic particles in chewable tablets.

What was recalled

GOODSENSE Ultra Strength, Antacid TABLETS, Calcium Carbonate 1000 mg, 72 Chewable Tablets, Distributed by: Geiss, Destin & Dunn, inc., Peachtree City, GA, NDC 50804-171-68.

Recalling firm
Guardian Drug Co. Inc.
NDC code
50804-171-68
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0575-2026

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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Class II · Moderate risk Ongoing

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Reason Presence of foreign substance: small metallic particles in chewable tablets.

Guardian Drug Co. Inc. NDC 76162-129-68 D-0579-2026
Class II · Moderate risk Ongoing

TopCare health

Reason Presence of foreign substance: small metallic particles in chewable tablets.

Guardian Drug Co. Inc. NDC 76162-128-22 D-0578-2026
Class II · Moderate risk Ongoing

EQUALINE ultra strength

Reason Presence of foreign substance: small metallic particles in chewable tablets.

Guardian Drug Co. Inc. NDC 41163-171-68 D-0577-2026
Class II · Moderate risk Ongoing

EQUALINE extra strength

Reason Presence of foreign substance: small metallic particles in chewable tablets.

Guardian Drug Co. Inc. NDC 41163-129-22 D-0576-2026
Class II · Moderate risk Ongoing

GOODSENSE Extra Strength

Reason Presence of foreign substance: small metallic particles in chewable tablets.

Guardian Drug Co. Inc. NDC 50804-129-22 D-0574-2026