CLASS II Drug recall · Reported 30 Sep 2020 · FDA Enforcement Report

Nature-Throid, 1 Grain, 65 mg (Thyroid U.S.P. 1 gr. recalled

Preferred Pharmaceuticals is recalling Nature-Throid, 1 Grain, 65 mg (Thyroid U.S.P. 1 gr. (65mg)/Liothyronine (T3), distributed in California, Georgia. The recall was initiated on 2 Sep 2020 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesa) Lot #: A0220Q, Exp. Date: 10/31/2020; b) Lot #: K15171, Exp. Date: 10/31/2020
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-1623-2020
FDA event ID
86394
Recalling firm
Preferred Pharmaceuticals, Anaheim, CA
Classification
Class II
Status
Terminated
Recall initiated
2 Sep 2020
FDA classified
24 Sep 2020
Reported
30 Sep 2020
Type
Voluntary: Firm initiated
Customers notified by
Letter

Timeline

2 Sep 2020Recall initiated by company
24 Sep 2020Classified by FDA+22 days
30 Sep 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

Product as listed by the FDA

Nature-Throid, 1 Grain, 65 mg (Thyroid U.S.P. 1 gr. (65mg)/Liothyronine (T3) 9mcg/Levothyroxine (T4) 38mcg, packaged in a) 90-count bottles (NDC 68788-7604-09), b) 100-count tablets (NDC 68788-7604-01), Rx Only, Mfg: RLC Labs; Cave Creek, AZ, Preferred Pharmaceuticals, Inc.

Where it was distributed

Repackaged tablets sold to three physicians located in CA and GA.

CaliforniaGeorgia

Questions about this recall

Why was it recalled?

CGMP Deviations

Which lots are affected?

a) Lot #: A0220Q, Exp. Date: 10/31/2020; b) Lot #: K15171, Exp. Date: 10/31/2020

Where was it sold?

Repackaged tablets sold to three physicians located in CA and GA.

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

3 other products · FDA event 86394

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