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FDA (US) · MEDWATCH SAFETY ALERTAugust 13, 2026
Intravascular Administration Set Recall: Baxter Removes Duo-Vent Solution Sets
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Item details are published by the U.S. FDA on fda.gov; SPEQ surfaces them for reference and is not affiliated with or endorsed by the FDA. The authoritative notice is on fda.gov.
Item type
MedWatch Safety Alert
Published
August 13, 2026
Source
U.S. FDA (MedWatch / press releases)
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The complete FDA notice — the affected products, the action required, and any recall detail — is published on fda.gov. SPEQ surfaces and indexes it for reference; the authoritative notice lives on fda.gov.
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