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      <constitutionalAuthorityStatementText>&lt;pre&gt;[Congressional Record Volume 169, Number 153 (Thursday, September 21, 2023)][House]From the Congressional Record Online through the Government Publishing Office [&lt;a href="https://www.gpo.gov"&gt;www.gpo.gov&lt;/a&gt;]By Ms. SCHAKOWSKY:H.R. 5662.Congress has the power to enact this legislation pursuantto the following:Section 8 of article 1 of the ConstitutionThe single subject of this legislation is:To require FDA to establish an electronic format formedical device recall notification to expediate the recallinformation dissemination process.[Page H4459]&lt;/pre&gt;</constitutionalAuthorityStatementText>
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        <title>Medical Device Recall Improvement Act</title>
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    <title>Medical Device Recall Improvement Act</title>
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        <title>To improve medical device recall notifications by amending the Federal Food, Drug, and Cosmetic Act to establish an electronic format for device recall notifications, and for other purposes.</title>
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      <actionDate>2023-09-22</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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