Thyroid, USP, Rx only, Net Wt: 0.50kg, For Manufacturing, Processing or Repackaging Use Only, Specialty Process Labs, Phoenix, AZ…
Reason Subpotent Drug
68 FDA recalls mention Thyroid. The most recent are listed below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Thyroid.
Reason Subpotent Drug
Reason Failed Stability Specifications
Reason Failed Stability Specifications
Reason Lack of sterility assurance
Reason CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Reason Subpotent Drug
Reason Subpotent Drug
Reason Subpotent Drug
Reason Subpotent Drug
Reason Subpotent Drug
Reason Subpotent Drug: FDA analysis found these products to be less than the labeled claim for the levothyroxine (T4) portion of the product.
Reason Subpotent Drug: FDA analysis found these products to be less than the labeled claim for the levothyroxine (T4) portion of the product.
Reason CGMP deviations; repackaged product was recalled by the manufacturer because it was manufactured under the same conditions as products found to be…
Reason CGMP Deviations
Reason CGMP Deviations
Reason CGMP Deviations
Reason CGMP Deviations
Reason Subpotent Drug: FDA analysis found product to be subpotent
Reason Subpotent Drug: FDA analysis found product to be subpotent
Reason Subpotent Drug: FDA analysis found product to be subpotent
Reason Subpotent Drug: FDA analysis found product to be subpotent
Reason Subpotent Drug: FDA analysis found product to be subpotent
Reason Subpotent Drug: FDA analysis found product to be subpotent
Reason CGMP Deviations: manufactured under the same conditions as those found to be subpotent.
Reason CGMP Deviations: manufactured under the same conditions as those found to be subpotent.
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