88S31264 BPG-D
 
  By: LaMantia S.R. No. 79
 
 
 
R E S O L U T I O N
         WHEREAS, In January 2020, the Food and Drug Administration
  issued industry guidance outlining its enforcement priorities
  regarding e-cigarettes, vapes, and other electronic nicotine
  delivery system products; and
         WHEREAS, This guidance emphasized the agency's focus on
  enforcing regulations against all flavored, cartridge-based ENDS
  products, but it unintentionally created a loophole, exempting all
  disposable vaping products from enforcement for nearly three years;
  and
         WHEREAS, Since January 2020, a significant influx of illicit
  disposable vaping products has entered the United States; these
  originate primarily in China and mostly feature flavors designed to
  appeal to children; and
         WHEREAS, According to the Centers for Disease Control and
  Prevention's National Youth Tobacco Survey, youth consumption of
  disposable vaping products has surged by an alarming 2,188 percent
  since 2019; a substantial majority of disposable vaping products
  introduced to the market have either entered after the FDA's
  regulatory submission cutoff date of August 8, 2016, or have failed
  to comply with the FDA's regulatory pathways designed to ensure
  that products available in stores promote public health and safety;
  the urgency of this matter is reinforced by the fact that, in 2021,
  46 percent of high school e-cigarette users vaped at least 20 days a
  month, and over 30 percent reported vaping every day; and
         WHEREAS, The continued rise in youth vaping is a serious
  public health concern that demands immediate attention and action;
  much-needed measures include the publication of a directory of
  disposable vapor products that can be sold subject to FDA
  enforcement discretion, allowing retailers to remove all illegal
  disposable vapor products from shelves, as well as the allocation
  of resources for federal enforcement across all jurisdictions and
  at all ports and border control points of entry; now, therefore, be
  it
         RESOLVED, That the Senate of the 88th Texas Legislature, 3rd
  Called Session, hereby urge the Food and Drug Administration to
  provide clear enforcement guidance regarding the distribution and
  sales of disposable vapor products; and, be it further
         RESOLVED, That the Secretary of the Senate forward official
  copies of this resolution to the President of the United States, to
  the Speaker of the House of Representatives and the President of the
  Senate of the United States Congress, to the Commissioner of the
  FDA, and to all the members of the Texas delegation to Congress with
  the request that this resolution be officially entered in the
  Congressional Record as a memorial to the Congress of the United
  States of America.