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FDA inspected Totowa8217;s Riverview Drive facility early in 2008 and found that the company had significant cGMP violations and continued to manufacture unapproved drugs. FDA has issued 483s to the facility based upon past inspections that revealed the companys failure to investigate serious adverse event reports about some of its products, as well as a host of cGMP improprieties at the facilities including shoddy Quality Control and even one instance of, yes, duct tape being used to keep powder from leaking during production. In the summer of 2008, FDA forced the company to initiate a voluntary recall of all its products, from oxycodone to prenatal vitamins, as a precautionary action since the conditions under which the products were manufactured could not be verified as safe. As part of the Consent Decree, Activis must destroy any remaining recalled drugs still in its possession. 8220;The FDA will not allow manufacturers to put the public8217;s health at risk,8221; says Janet Woodcock, M.

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