CLASS II Drug recall · Reported 26 Aug 2020 · FDA Enforcement Report

Thyroid 1 Grain Tablets, 28-count bags recalled

Calvin Scott & Company is recalling Thyroid 1 Grain Tablets, 28-count bags, distributed nationwide in the US. The recall was initiated on 27 Jul 2020 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot #: 19233; Exp. Date: 08/20; 19254, Exp. Date 09/20; 19273, Exp. Date: 1/21
Quantity recalledN/A

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-1517-2020
FDA event ID
86123
Recalling firm
Calvin Scott & Company, Albuquerque, NM
Classification
Class II
Status
Terminated
Recall initiated
27 Jul 2020
FDA classified
20 Aug 2020
Reported
26 Aug 2020
Type
Voluntary: Firm initiated
Customers notified by
E-Mail

Timeline

27 Jul 2020Recall initiated by company
20 Aug 2020Classified by FDA+24 days
26 Aug 2020Published 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

CGMP Deviations: Light sensitive drug products repackaged in transparent/partially transparent pouches.

Product as listed by the FDA

Thyroid 1 Grain Tablets, 28-count bags, Distributed by: Calvin Scott & Co., Inc. Albuquerque, NM 87123, Manufactured by RLC Labs, Cave Creek, AZ 85331, NDC 64727-3300-02

Where it was distributed

Nationwide within the United States

Nationwide

Questions about this recall

Is Thyroid 1 Grain Tablets, 28-count bags recalled?

Yes. Calvin Scott & Company recalled Thyroid 1 Grain Tablets, 28-count bags on 27 Jul 2020. The recall is Class II and its status is Terminated. Recall number D-1517-2020.

Why was it recalled?

CGMP Deviations: Light sensitive drug products repackaged in transparent/partially transparent pouches.

Which lots are affected?

Lot #: 19233; Exp. Date: 08/20; 19254, Exp. Date 09/20; 19273, Exp. Date: 1/21

Where was it sold?

Nationwide within the United States

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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