CLASS II Food recall · Reported 6 Aug 2014 · FDA Enforcement Report

Calcium Formula, 250 cc HDPE recalled by GM Manufacturing

GM Manufacturing is recalling Calcium Formula, 250 cc HDPE, distributed in California. The recall was initiated on 3 Jul 2014 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesEXP08.2016
Quantity recalled501 units

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-2256-2014
FDA event ID
68717
Recalling firm
GM Manufacturing, Gardena, CA
Brand
Calcium
Classification
Class II
Status
Terminated
Recall initiated
3 Jul 2014
FDA classified
31 Jul 2014
Reported
6 Aug 2014
Type
Voluntary: Firm initiated
Customers notified by
Letter
Product category
Other

Timeline

3 Jul 2014Recall initiated by company
31 Jul 2014Classified by FDA+28 days
6 Aug 2014Published in enforcement report+6 days

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

Reason for recall

GM Manufacturing is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.

Product as listed by the FDA

Calcium Formula, 250 cc HDPE Bottles

Where it was distributed

CA

California

Questions about this recall

Is Calcium Formula, 250 cc HDPE recalled?

Yes. GM Manufacturing recalled Calcium Formula, 250 cc HDPE on 3 Jul 2014. The recall is Class II and its status is Terminated. Recall number F-2256-2014.

Why was it recalled?

GM Manufacturing is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.

Which lots are affected?

EXP08.2016

Where was it sold?

CA

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

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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