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15, 2007, do not need to submit premarket applications (unless the products were since modified). 3The numbers provided for SE and EX REQ marketing orders are for a combination of originally-regulated and deemed products. 4Regardless of tobacco product type 5In addition to the reasons stated in the text, products were also excluded from the list if for example a product received a Refuse to Accept or Refuse to File letter from FDA, if the application was withdrawn by the applicant, or if the application was administratively closed prior to the posting of the list.

In other words, the defendants argued that, having complied with the federal warning requirements, they could not be held liable for the plaintiff's mother's death, even if everything the plaintiff asserted was true

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