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=”https://dawamedical.com/wp-content/uploads/2021/07/Medtronic-Vascular-Recalls-Angiographic-Guidewire-Component-Due-to-Being-Non-sterile-_-FDA.pdf” title=”Medtronic Vascular Recalls Angiographic Guidewire Component Due to Being Non-sterile _ FDA”]
