FDA recall record

Preferred Pharmaceuticals Nature-Throid, 1 Grain, 65 mg recall — FDA D-1623-2020

CGMP Deviations

Class IIclassification
D-1623-2020official record ID
Sep 30, 2020report date

Recall record at a glance

Official recordD-1623-2020
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmPreferred Pharmaceuticals, Inc.
Report dateSep 30, 2020
Recall initiation dateSep 2, 2020
QuantityN/A
LocationAnaheim, CA, United States

Official product description

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.

Why the product was recalled

CGMP Deviations

Distribution information

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

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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