On the recordSeptember 21, 2023
Madam President, I ask unanimous consent that the text of the bill be printed in the Record. There being no objection, the text of the bill was ordered to be printed in the Record, as follows: S. 2907 Be it enacted by the Senate and House of Representatives of the United States of America in Congress assembled, SECTION 1. SHORT TITLE. This Act may be cited as the ``Medical Device Recall Improvement Act''. SEC. 2. REGULATION OF MEDICAL DEVICE RECALLS. Chapter V of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 351 et seq.), is amended by inserting after section 518A of such Act the following: ``SEC. 518B. ELECTRONIC NOTIFICATION FORMAT FOR DEVICE RECALLS. ``(a) Electronic Notification Format for Device Recalls.-- ``(1) In general.--Not later than 2 years after the date of enactment of the Medical Device Recall Improvement Act, the Secretary shall publish a form and manner for notifications of a recall.…
Source
govinfo.gov
