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Update on Risk of Type III Endoleaks with Use of Endologix AFX Endovascular AAA Graft Systems - FDA Safety Communication
Oscor Inc. Issues Voluntary Worldwide Recall of Destino Twist Steerable Guiding Sheath Due to the Risk of the Device Hub Cap and Seal on the Proximal End of the Device Handle Detachment During Use
Stop Using LuSys Laboratories COVID-19 Tests: FDA Safety Communication
Field Safety Notices: 3 to 7 January 2022
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