Recall for Medtronic Vascular Angiographic Guidewire Component

Serious injuries or death may result from the use of these devices. The FDA has identified this as a Class I recall, the most serious type o

If your email program has trouble displaying this email, view as a webpage. Medtronic Vascular Recalls Angiographic Guidewire Component Due to Risk of Being Non-sterile   Medtronic Vascular is recalling their Angiographic Guidewire Component because certain 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.    Read More The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death.   Questions?  If you have questions about this recall, contact the Division of Industry and Consumer Education (DICE).

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