Medical Device Recall Improvement Act

Cost and committee reports

Official records Congress.gov attaches to H.R. 5662.

• Constitutional authority statementThe sponsor’s statement of where the Constitution gives Congress the power to pass this bill. Statement by Ms. SCHAKOWSKY, as printed in the Congressional Record (Vol. 169, No. 153, September 21, 2023, Page H4459):
  Section 8 of article 1 of the Constitution The single subject of this legislation is: To require FDA to establish an electronic format for medical device recall notification to expediate the recall information dissemination process.
  Source: Congress.gov, Congressional Record September 21, 2023 ↗

  Evidence

  Field in the Congress.gov record

  constitutionalAuthorityStatementText

  Statement length

  232 characters

  Congress.gov bill record

  H.R. 5662, 118th Congress

  Congress.gov API record

  https://api.congress.gov/v3/bill/118/hr/5662

  Record last updated by Congress.gov

  December 5, 2025

  PORKER copy retrieved

  September 14, 2026

  Stored copy, SHA-256 of the file

  372e4bb9757340b04c08616ada93c8f00257058b5cc41e6b5f8ac96642001704

  PORKER shows the statement exactly as printed, with the page markup removed. It is the sponsor’s claim; it is not a legal finding.

Congress.gov’s record for this bill does not list a CBO cost estimate or a committee report (as of December 5, 2025). Not every bill gets one.

From the Congress.gov bill record for H.R. 5662, last updated December 5, 2025. PORKER’s copy was retrieved September 14, 2026 and is refreshed nightly. Open “Evidence” on any line for the record, field and file fingerprint.