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Anti-anxiety med withdrawn due to "foreign substance" and risk of infection



The company stated that the likelihood of someone getting ill "is expected to be rare, but the remote risk of contracting a patient cannot be ruled out." Milan added that he did not receive any reports of adverse events related to this particular batch by Friday's announcement.

  Anxiety medicines are recalled

Milan refused to provide additional information about the product or the foreign substance.

The voluntary download includes one batch of bottles, each containing 500 0.5 mg tablets, which were distributed in the United States between July and August. The batch number affected is 8082708 and the expiration date is set to September 2020.

Instructions for wholesalers, retailers and consumers to return withdrawn bottles can be found in the company's announcement, which was also published in US Food and Drug Administration. website. Adverse events can be reported in the MedWatch Adverse Side Event Reporter.

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