Levothyroxine Sodium Tablets, USP, 150 mcg (0.0150 mg), 10 Tablets (10 x 1) unit dose blisters per carton, Rx only, Packaged and…
Reason Subpotent Drug
173 FDA recalls mention Levothyroxine. The most recent are listed below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Levothyroxine.
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Reason Product Mix-Up: A single bottle of this lot was reported by a pharmacy to contain 88 mcg tablets instead of 150 mcg tablets.
Reason Subpotent: During long term stability testing of Levothyroxine Sodium Tablets USP for 88 mcg, the assay content was observed below the approved…
Reason Subpotent drug
Reason Subpotent Drug: Assay below the approved specification
Reason Subpotent Drug: Assay below the approved specification
Reason Subpotent Drug: Assay below the approved specification
Reason Subpotent Drug: Assay below the approved specification
Reason Subpotent Drug: Assay below the approved specification
Reason Subpotent Drug: Assay below the approved specification
Reason Subpotent Drug: Assay below the approved specification
Reason Presence of a foreign substance: black hair found embedded in tablet.
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