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Food and Drug Administration.Convert timezones and find the best time for your meeting in This recall is being conducted with the knowledge of the U.S.
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Regular Mail or Fax: Download form or call 1-80 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-80.Complete and submit the report Online:.Patients should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this product.Īdverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax. The necessary form to document product information, as well as other information regarding this recall, is available at Consumers or healthcare workers with any questions regarding this recall can contact the customer call center (866) 625- 1618 M-F, 8am-7pm CST. Healthcare/distributors/retailers that have product which is being recalled should stop using product and return the recalled product. Customers who may have further distributed this product have been requested to identify their customers and notify them at once of this product recall. Customers that have Levetiracetam Injection, USP 500mg per 5 mL, which is being recalled, have been instructed to examine their inventory immediately and to quarantine, discontinue distribution of, and return as directed the recalled lots of product.
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is notifying customers by fax, email, FedEx, and/or certified mail, which includes arrangements for return of all recalled product.