When I went to the website, the image below is what is current today so I am guessing there may be more coming as the products to be recalled will need some type of listing for the products that the FDA listed as non approved. BD
The Food and Drug Administration (FDA) entered a consent decree of permanent injunction against Deltex Pharmaceuticals Inc. a Fort Bend County drug maker, based on "a history of significant violations," including manufacturing and distributing unapproved, adulterated and misbranded drugs.
The FDA originally requested a permanent injunction against Deltex and its president, Kabir Ahmed, and vice president, Mohidur R. Khan, because the company allegedly failed to obtain approval for its prescription drugs, failed to comply with federal regulations governing over-the-counter drugs and did not adhere to good manufacturing practices. It conducted a number of inspections in 2008 where it found numerous violations regarding quality control procedures and laboratory testing. The FDA alleged that it made several recommendations to correct these problems, but they were not followed.As part of the consent decree, Deltex will also recall and destroy all drugs produced and distributed since Oct. 31, 2008, and inform customers of the recall. The warning will cover all the unapproved drugs intended for treating cold, flu, allergies and coughs, including Tannate Pediatric Suspension, DuohistTM DH Liquid, Ed-A-Hist DM and Bromphenex DM
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