device recall
saveMedtronic Perfusion Systems device recall (Cls II)
October 20, 2025updated 3mo ago
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Medtronic HR-ACT (High Range Activated Clotting Time Cartridges), REF 402-03 — Reason: Medtronic personnel observed trace amounts of dry blood on the external carton label and Instructions for Use (IFU) in five boxes of one lot of ACT Cartridges. — Status: Ongoing
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