FDA recall record

Levothyroxine Sodium Tablets, USP 112 mcg, 90 tablets per bottle recall — FDA D-0353-2023

Sub-Potent Drug: Out of specification for assay at the 24 month interval.

Class IIclassification
D-0353-2023official record ID
Mar 8, 2023report date

Recall record at a glance

Official recordD-0353-2023
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmAlvogen, Inc.
Report dateMar 8, 2023
Recall initiation dateFeb 6, 2023
Quantity21,276 bottles
LocationMorristown, NJ, United States

Official product description

Levothyroxine Sodium Tablets, USP 112 mcg, 90 tablets per bottle, Rx Only, Manufactured by Lloyd Inc., Shenandoah, IA, 51601, Distributed by: Alvogen Inc, Pine Brook, NJ 07058, NDC 47781-654-90.

Why the product was recalled

Sub-Potent Drug: Out of specification for assay at the 24 month interval.

Distribution information

Nationwide and Puerto Rico.

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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