Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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Is Levothyroxine recalled?

Yes — there is an active recall. 62 ongoing FDA recalls mention Levothyroxine (186 total). Check the affected lots below.

Recalls are matched by product description. A recall usually affects specific lots, not every package of Levothyroxine. “Active” means an FDA recall is still ongoing; “closed” means it was terminated or completed. Checked against openFDA on Oct 10, 2026.

Levothyroxine recalls on record

none so far in 2026; 186 on record, newest first
Class II · Moderate risk

Levothyroxine Sodium Tablets

Product Mix-Up: A single bottle of this lot was reported by a pharmacy to contain 88 mcg tablets instead of 150 mcg tablets.

Ongoing Labeling / mix-up Alvogen, Inc D-0259-2026
Class II · Moderate risk

Levothyroxine Sodium Tablets

Subpotent: During long term stability testing of Levothyroxine Sodium Tablets USP for 88 mcg, the assay content was observed below the approved specification range.

Ongoing Wrong potency / content Accord Healthcare, INC. NDC 16729-450-15 D-0006-2026
Class II · Moderate risk

Levothyroxine Sodium Tablets

Failed Impurities/Degradation Specifications: Out of specifications result observed in the drug substance for impurity test during 3-month long term stability study.

Terminated Impurity / degradation Lupin Pharmaceuticals Inc. NDC 68180-967-03 D-0167-2025