CLASS II ONGOING Drug recall · Reported 10 Jun 2026 · FDA Enforcement Report

Discount drug mart, Extra Strength, Antacid Tablets recalled

Guardian Drug Co is recalling Discount drug mart, Extra Strength, Antacid Tablets, Calcium Carbonate 750 mg, distributed nationwide in the US. The recall was initiated on 28 May 2026 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot #: 1276118, Exp 1/31/2029.

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-0567-2026
FDA event ID
99098
Recalling firm
Guardian Drug Co, Dayton, NJ
Classification
Class II
Status
Ongoing
Recall initiated
28 May 2026
FDA classified
3 Jun 2026
Reported
10 Jun 2026
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Particulate Matter

Timeline

28 May 2026Recall initiated by company
3 Jun 2026Classified by FDA+6 days
10 Jun 2026Published in enforcement report+7 days

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

Reason for recall

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

Product as listed by the FDA

DISCOUNT drug mart, EXTRA STRENGTH, ANTACID TABLETS, Calcium Carbonate 750 mg, 96 Tablets, Distributed by: Drug Mart- Food Fair Medina, OH 44256, UPC: 0 93351 03992 8.

Where it was distributed

U.S.A. Nationwide

Nationwide

Questions about this recall

Is Discount drug mart, Extra Strength, Antacid Tablets, Calcium Carbonate 750 mg recalled?

Yes. Guardian Drug Co recalled Discount drug mart, Extra Strength, Antacid Tablets, Calcium Carbonate 750 mg on 28 May 2026. The recall is Class II and its status is Ongoing. Recall number D-0567-2026.

Why was it recalled?

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

Which lots are affected?

Lot #: 1276118, Exp 1/31/2029.

Where was it sold?

U.S.A. 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 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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