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Medtronic Vascular is recalling the Angiographic Guidewire Component because devices were not sterilized before being shipped directly to hospitals. If patients are exposed to the non-sterile device, serious adverse events could occur such as infection, sepsis, and death.

[pdf-embedder url=”” title=”Medtronic Vascular Recalls Angiographic Guidewire Component Due to Being Non-sterile _ FDA”]