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Cordis US Corp Recalls INFINITI Angiographic Catheter due to Products Being Shipped Without Undergoing Sterilization Procedures
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 ....
Adverse Event Reporting Program
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Drug Administration
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Cordis Us Corp
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Urgent Medical Device Recall Notice
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Urgent Medical Device Recall
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Acknowledgement Form
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Cordis Customer Support
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