CLASS II Drug recall · Reported 25 Mar 2015 · FDA Enforcement Report

Antacid Liquid Regular Strength Antacid & Anti-Gas recalled

Tarmac Products is recalling Antacid Liquid Regular Strength Antacid & Anti-Gas (Aluminum hydroxide 200 mg, Magnesium, distributed nationwide in the US. The recall was initiated on 6 Feb 2015 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot #: 7599 (Refer to lot 13L0009), 7600 (Refer to lot 13K0014), 7622 (Refer to lot 13L0008), 7623 (Refer to lot 13K0015), Exp 10/15
Quantity recalled78,591 bottles

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-0419-2015
FDA event ID
70577
Recalling firm
Tarmac Products, Miami Gardens, FL
Classification
Class II
Status
Terminated
Recall initiated
6 Feb 2015
FDA classified
18 Mar 2015
Reported
25 Mar 2015
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Sterility

Timeline

6 Feb 2015Recall initiated by company
18 Mar 2015Classified by FDA+40 days
25 Mar 2015Published 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

Microbial Contamination of Non-Sterile Products: Lots failed microbiological testing at the 12-month time point.

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

Antacid Liquid Regular Strength Antacid & Anti-Gas (Aluminum hydroxide 200 mg, Magnesium hydroxide 200 mg, Simethicone 20 mg (in each 5 mL, 1 teaspoon), Mint flavor, 12 fl oz (355 mL) bottle, Distributed By: Walgreen Co., 200 Wilmot Rd., Deerfield, IL 60015, NDC 0363-0073-02, UPC 3 11917 15114 4.

Where it was distributed

Nationwide

Nationwide

Questions about this recall

Why was it recalled?

Microbial Contamination of Non-Sterile Products: Lots failed microbiological testing at the 12-month time point.

Which lots are affected?

Lot #: 7599 (Refer to lot 13L0009), 7600 (Refer to lot 13K0014), 7622 (Refer to lot 13L0008), 7623 (Refer to lot 13K0015), Exp 10/15

Where was it sold?

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 26 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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