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Incorrect Label Potency Leads to Thyroid Drug Recall

Acella Pharmaceuticals has recalled its thyroid medication for the third time in a year over potency issues. Tim HayesContributing Editor, Healthcare Packaging Healthcare Packaging May 14th, 2021 A recent WebMDarticle discussed a nationwide thyroid drug recall linked to incorrect information on the label. The drug in question is Acella Pharmaceuticals’ NP Thyroid medication intended to treat hypothyroidism. During routine testing, the affected lots were found to contain less than 90% of the two ingredients listed on the label: liothyronine and levothyroxine. At least 43 adverse events have been reported in relation to the drug, which could be linked to the recall. This is the third recall related to this particular drug’s potency in the past year. Back in November, the potency was too low, and last May it was overly potent. 

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Some Thyroid Drugs Recalled Over Reduced Potency

The recalled drugs were found to contain less than 90% of the drug s two labeled ingredients to treat hypothyroidism.

Some NP Thyroid Lots Recalled Due to Reduced Potency

Some NP Thyroid Lots Recalled Due to Reduced Potency
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Thyroid Medicine Gets Third Major Recall Over Lack of

Thyroid Medicine Gets Third Major Recall Over Lack of
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