FDA Drug recall D-0353-2023
Levothyroxine Sodium Tablets, USP 112 mcg, 90 tablets per bottle, Rx Only, Manufactured by Lloyd Inc., Shenandoah, IA, 51601, Distributed b…
- FDA Drug
- Class II
- terminated
- Published 2023-03-08
On 2023-03-08 the FDA classified a Class II recall of Levothyroxine Sodium Tablets, USP 112 mcg, 90 tablets per bottle, Rx Only, Manufactured by Lloyd Inc., Shenandoah, IA, 51601, Distributed b… by Alvogen, citing sub-Potent Drug: Out of specification for assay at the 24 month interval.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0353-2023 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2023-02-06 |
| Published | 2023-03-08 |
| Last updated | 2026-09-13 11:52 UTC |
| Company | Alvogen |
| Distribution | US |
Product
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.
Reason
Sub-Potent Drug: Out of specification for assay at the 24 month interval.
Identifiers
| ndc | 47781-640-90 |
|---|---|
| ndc | 47781-640-10 |
| ndc | 47781-643-90 |
| ndc | 47781-643-10 |
| ndc | 47781-646-90 |
| ndc | 47781-646-10 |
| ndc | 47781-649-90 |
| ndc | 47781-649-10 |
| ndc | 47781-651-90 |
| ndc | 47781-651-10 |
| ndc | 47781-654-90 |
| ndc | 47781-654-10 |
| ndc | 47781-657-90 |
| ndc | 47781-657-10 |
| ndc | 47781-659-90 |
| ndc | 47781-659-10 |
| ndc | 47781-662-90 |
| ndc | 47781-662-10 |
| ndc | 47781-665-90 |
| ndc | 47781-665-10 |
| ndc | 47781-668-90 |
| ndc | 47781-668-10 |
| ndc | 47781-671-90 |
| ndc | 47781-671-10 |
| ndc | 47781-728-90 |
| ndc | 47781-721-90 |
| code_info | Lot # HE02221, Exp. 05/2023 |
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0353-2023%22
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