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This bill directs the Secretary of Defense to develop and implement a plan within 180 days to identify and replace medical syringes in Department of Defense inventories and acquisitions that have been subject to FDA Import Alerts or FDA Safety Communications. The plan requires replacing affected syringes with those produced domestically or by U.S. partners and allies, and establishes processes for ongoing tracking and replacement of problematic syringes. The Secretary must report to Congress on the number of affected syringes, planned acquisitions, product details, and implementation procedures.
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