FDA - Food and Drug Administration

10/18/2024 | Press release | Distributed by Public on 10/18/2024 18:44

Medtronic (MiniMed™ 600 series or 700 series insulin pumps/Medtronic plc) Recall reason: Device & Drug Safety - Defect

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FDA - Food and Drug Administration published this content on October 18, 2024, and is solely responsible for the information contained herein. Distributed via Public Technologies (PUBT), unedited and unaltered, on October 19, 2024 at 00:44 UTC. If you believe the information included in the content is inaccurate or outdated and requires editing or removal, please contact us at [email protected]