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Medline recalls acetaminophen tablets
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Medline Industries Inc. has initiated a voluntary recall of acetaminophen tablets, according to the FDA.
The 500 mg uncoated, compressed tablets, part of lot 45810, have been mislabeled as 325 mg. According to the FDA, the tablets are packaged in 100 tablet bottles with the following numbers: "Medline Item Number: OTC20101, NDC#: 53329-641-30."
As detailed in the release, the error is not easily identifiable and taking the acetaminophen as instructed may lead to liver failure or liver toxicity.
Medline has notified retailers, consumers and distributors, according to the release. The company is arranging for return and credit of the tablets, which were distributed nationwide from June 12 to Sept. 18, 2015.
Consumers can contact recalls@medline.com or 856-359-1704 with questions about the recall. Any adverse reactions or issues in regards to the product can be reported to the FDA's MedWatch Adverse Event Reporting program.