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A-S Medication Recalls Acetaminophen Extra Strength Tablets Over Mislabeling

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A-S Medication Solutions, LLM (ASM) is recalling Acetaminophen Extra Strength tablets contained in Health Essentials Kits due to an incomplete prescription drug labeling.

The Acetaminophen Extra Strength Tablet is an over-the-counter (OTC) product that is used as a pain and fever reliever.

Over 198,350 100-count bottles of Acetaminophen Extra Strength 500 mg Tablets have been recalled as they lack the full OTC Drug Facts chart. If the safety warnings on the OTC label are not followed, the use of acetaminophen could be potentially dangerous.

The recalled products are labeled with NDC 50090-5350-0 and are packaged in white plastic bottles contained in a clear plastic bag with other seasonal products labeled as a Health Essentials Kits, which were distributed by Humana to its members.

The Health Kits were most likely distributed in the United States between January 14 and March 15, and their expiration dates are either 7/31/22 or 8/31/22.

Consumers and distributors who are having the affected product should stop using it and return it in preaddressed return mailers that will be provided by ASM or the distributors.

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