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Urgent Field Safety Notice Commercial name of the affected product: Inferior Vent Cave (IOC) Filter Manufacturer : William Cook Europe Cook Reference Number: 2019FA0001 Type of action: Field Safety
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Contact the manufacturer of your IVC filter to see if there have been any recalls or safety issues reported.
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Provide any information requested by the manufacturer, such as the model and lot number of your IVC filter.
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Follow any instructions given by the manufacturer for returning or replacing the recalled IVC filter.

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Patients who have received an IVC filter and are concerned about potential recalls or safety issues.
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Healthcare providers who have treated patients with IVC filters and want to ensure the safety of their patients.
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IVC filter recallsmanufacturers CR refers to the process of reporting recalls related to Inferior Vena Cava (IVC) filters by manufacturers to the appropriate regulatory agencies.
Manufacturers of IVC filters are required to file recalls related to their products.
To fill out IVC filter recallsmanufacturers CR, manufacturers must provide specific information about the recalled products, reasons for the recall, and any adverse events associated with the products.
The purpose of IVC filter recallsmanufacturers CR is to ensure the safety and efficacy of IVC filters by promptly addressing any issues or defects that may arise.
The information that must be reported on IVC filter recallsmanufacturers CR includes details of the recalled products, reasons for the recall, any adverse events reported, and actions taken to address the issue.
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