CLASS II Drug recall · Reported 25 May 2022 · FDA Enforcement Report

Magnesium Hydroxide 1200mg, Aluminum Hydroxide 1200mg recalled

Plastikon Healthcare is recalling Magnesium Hydroxide 1200mg, Aluminum Hydroxide 1200mg, Simethicone 120mg cup, distributed in Indiana. The recall was initiated on 24 Mar 2022 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot: 20042A, 20043A, 20045A, 20046A, 20047A, EXP May 2022
Quantity recalled106,400 Unit Dose cups

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-0871-2022
FDA event ID
89879
Recalling firm
Plastikon Healthcare, Lawrence, KS
Classification
Class II
Status
Completed
Recall initiated
24 Mar 2022
FDA classified
13 May 2022
Reported
25 May 2022
Type
Voluntary: Firm initiated
Customers notified by
Press Release

Timeline

24 Mar 2022Recall initiated by company
13 May 2022Classified by FDA+50 days
25 May 2022Published in enforcement report+12 days

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

Reason for recall

CGMP Deviations: Failure to properly investigate failed microbial testing.

Product as listed by the FDA

Magnesium Hydroxide 1200mg, Aluminum Hydroxide 1200mg, Simethicone 120mg, 30 mL cup, packaged in 10 cups per tray, 10 trays per carton, For Institutional Use Only, Distributed by Major Pharmaceuticals, Livonia, MI 48152, NDC: 0904-6838-73.

Where it was distributed

Distributed in Indiana for further distribution in the USA.

Indiana

Questions about this recall

Why was it recalled?

CGMP Deviations: Failure to properly investigate failed microbial testing.

Which lots are affected?

Lot: 20042A, 20043A, 20045A, 20046A, 20047A, EXP May 2022

Where was it sold?

Distributed in Indiana for further distribution in the USA.

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.

Other products in this recall event

4 other products · FDA event 89879

This product is part of a recall event; the main page for the event is Magnesium Hydroxide 1200mg, Aluminum Hydroxide 1200mg recalled.

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