FDA Drug recall D-0403-2026
Levothyroxine Sodium Tablets USP 150 mcg, 1000 Tablets bottle, Rx Only, Manufactured for: Macleods Pharma USA, Inc., Princeton, NJ, Manufac…
- FDA Drug
- Class II
- ongoing
- Published 2026-04-01
On 2026-04-01 the FDA classified a Class II recall of Levothyroxine Sodium Tablets USP 150 mcg, 1000 Tablets bottle, Rx Only, Manufactured for: Macleods Pharma USA, Inc., Princeton, NJ, Manufac… by Macleods Pharma Usa, citing subpotent Drug.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0403-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2026-02-26 |
| Published | 2026-04-01 |
| Last updated | 2026-09-13 11:52 UTC |
| Company | Macleods Pharma Usa |
| Distribution | US |
Product
Levothyroxine Sodium Tablets USP 150 mcg, 1000 Tablets bottle, Rx Only, Manufactured for: Macleods Pharma USA, Inc., Princeton, NJ, Manufactured by: Macleods Pharmaceuticals Ltd., Sarigam, Valsad, Guajarat, INDIA NDC 33342-401-44
Reason
Subpotent Drug
Identifiers
| ndc | 33342-393-10 |
|---|---|
| ndc | 33342-393-11 |
| ndc | 33342-393-44 |
| ndc | 33342-394-10 |
| ndc | 33342-394-11 |
| ndc | 33342-394-44 |
| ndc | 33342-395-10 |
| ndc | 33342-395-11 |
| ndc | 33342-395-44 |
| ndc | 33342-396-10 |
| ndc | 33342-396-11 |
| ndc | 33342-396-44 |
| ndc | 33342-397-10 |
| ndc | 33342-397-11 |
| ndc | 33342-397-44 |
| ndc | 33342-398-10 |
| ndc | 33342-398-11 |
| ndc | 33342-398-44 |
| ndc | 33342-399-10 |
| ndc | 33342-399-11 |
| ndc | 33342-399-44 |
| ndc | 33342-400-10 |
| ndc | 33342-400-11 |
| ndc | 33342-400-44 |
| ndc | 33342-401-10 |
| ndc | 33342-401-11 |
| ndc | 33342-401-44 |
| ndc | 33342-402-10 |
| ndc | 33342-402-11 |
| ndc | 33342-402-44 |
| ndc | 33342-403-10 |
| ndc | 33342-403-11 |
| ndc | 33342-403-44 |
| ndc | 33342-404-10 |
| ndc | 33342-404-11 |
| ndc | 33342-404-44 |
| code_info | Lot 16240062A, exp date 3/2026 |
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0403-2026%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.