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    <updateDate>2019-11-15T21:18:26Z</updateDate>
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    <introducedDate>2005-03-17</introducedDate>
    <congress>109</congress>
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        <chamber>House</chamber>
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            <name>Health Subcommittee</name>
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                <name>Referred to</name>
                <date>2005-03-22T22:09:45Z</date>
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            <date>2005-03-17T15:06:10Z</date>
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        <title>Tim Fagan's Law</title>
        <congress>109</congress>
        <number>2345</number>
        <type>HR</type>
        <latestAction>
          <actionDate>2005-05-23</actionDate>
          <text>Referred to the Subcommittee on Health.</text>
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        <actionDate>2005-03-22</actionDate>
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        <text>Referred to the Subcommittee on Health.</text>
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        <actionDate>2005-03-17</actionDate>
        <text>Referred to the House Committee on Energy and Commerce.</text>
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            <name>Energy and Commerce Committee</name>
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        <actionDate>2005-03-17</actionDate>
        <text>Introduced in House</text>
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        <actionDate>2005-03-17</actionDate>
        <text>Introduced in House</text>
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    <sponsors>
      <item>
        <bioguideId>I000057</bioguideId>
        <fullName>Rep. Israel, Steve [D-NY-2]</fullName>
        <firstName>STEVE</firstName>
        <lastName>ISRAEL</lastName>
        <party>D</party>
        <state>NY</state>
        <district>2</district>
        <isByRequest>N</isByRequest>
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    <policyArea>
      <name>Health</name>
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    <subjects>
      <legislativeSubjects>
        <item>
          <name>Administrative remedies</name>
        </item>
        <item>
          <name>Commerce</name>
        </item>
        <item>
          <name>Communication in medicine</name>
        </item>
        <item>
          <name>Consumer protection</name>
        </item>
        <item>
          <name>Crime and Law Enforcement</name>
        </item>
        <item>
          <name>Criminal justice information</name>
        </item>
        <item>
          <name>Defective products</name>
        </item>
        <item>
          <name>Department of Health and Human Services</name>
        </item>
        <item>
          <name>Drug adulteration</name>
        </item>
        <item>
          <name>Drug industry</name>
        </item>
        <item>
          <name>Drugs</name>
        </item>
        <item>
          <name>Fines (Penalties)</name>
        </item>
        <item>
          <name>Food and Drug Administration (FDA)</name>
        </item>
        <item>
          <name>Government Operations and Politics</name>
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        <item>
          <name>Government paperwork</name>
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          <name>Governmental investigations</name>
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          <name>Informers</name>
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          <name>Intellectual property</name>
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        <item>
          <name>Labeling</name>
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        <item>
          <name>Law</name>
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        <item>
          <name>Medical personnel</name>
        </item>
        <item>
          <name>Product counterfeiting</name>
        </item>
      </legislativeSubjects>
      <policyArea>
        <name>Health</name>
      </policyArea>
    </subjects>
    <summaries>
      <summary>
        <versionCode>00</versionCode>
        <actionDate>2005-03-17</actionDate>
        <actionDesc>Introduced in House</actionDesc>
        <updateDate>2005-04-25T20:34:00Z</updateDate>
        <text><![CDATA[ <p>Counterfeit Drug Enforcement Act - Amends the Federal Food, Drug, and Cosmetic Act to direct the Secretary of Health and Human Services, upon a finding of reasonable probability that a drug intended for human use would cause serious health consequences or death, to issue an order requiring the appropriate person (including the manufacturers, importers, distributors, or retailers of the drug) to: (1) cease distribution of the drug; (2) notify health professionals of the order and instruct such professionals to cease administering or prescribing the drug; and (3) amend the order to include a recall if necessary.</p> <p>Establishes a criminal fine and/or imprisonment for a person who: (1) knowingly causes a prescription drug to be adulterated or misbranded and sells or trades the drug; or (2) purchases or trades for such drug knowing or having reason to know that the drug was knowingly adulterated or misbranded. Requires a manufacturer of a drug to notify the Secretary within 48 hours after first receiving or becoming aware of information that reasonably suggests that such a violation may have occurred. </p> <p>Increases funding for Food and Drug Administration (FDA) inspections, examinations, and investigations.</p>]]></text>
      </summary>
    </summaries>
    <title>Counterfeit Drug Enforcement Act</title>
    <titles>
      <item>
        <titleType>Short Titles as Introduced</titleType>
        <title>Counterfeit Drug Enforcement Act</title>
      </item>
      <item>
        <titleType>Display Title</titleType>
        <title>Counterfeit Drug Enforcement Act</title>
      </item>
      <item>
        <titleType>Official Title as Introduced</titleType>
        <title>To amend the Federal Food, Drug, and Cosmetic Act to establish recall authority regarding drugs, to increase criminal penalties for the sale or trade of prescription drugs knowingly caused to be adulterated or misbranded, and for other purposes.</title>
      </item>
    </titles>
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        <type>Introduced in House</type>
        <date>2005-03-17T05:00:00Z</date>
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    <latestAction>
      <actionDate>2005-03-22</actionDate>
      <text>Referred to the Subcommittee on Health.</text>
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    <dc:rights>Pursuant to Title 17 Section 105 of the United States Code, this file is not subject to copyright protection and is in the public domain.</dc:rights>
    <dc:contributor>Congressional Research Service, Library of Congress</dc:contributor>
    <dc:description>This file contains bill summaries and statuses for federal legislation. A bill summary describes the most significant provisions of a piece of legislation and details the effects the legislative text may have on current law and federal programs. Bill summaries are authored by the Congressional Research Service (CRS) of the Library of Congress. As stated in Public Law 91-510 (2 USC 166 (d)(6)), one of the duties of CRS is "to prepare summaries and digests of bills and resolutions of a public general nature introduced in the Senate or House of Representatives". For more information, refer to the User Guide that accompanies this file.</dc:description>
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