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Edwards Lifesciences, LLC: Medical Device Recalls in 2017

Updated on March 25, 2026.

According to to data from the FDA, there was 1 medical device recall made by Edwards Lifesciences, LLC in 2017. See the detail of the recall below.

You can see similar recalls for other firms.

Data Source: FDA.
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  • Fogarty Adherent Clot Catheter Model Numbers 1408010 and 140806 Product Usage: The Fogarty adherent clot catheters are designed to effectively remove clot material in the peripheral vasculature. The catheters are indicated for the removal of emboli and thrombi from native arteries or synthetic grafts. The device are designed to facilitate clots too resistant to be removed by an elastomeric balloon. The device features a spiral-shaped, latex-covered stainless steel cable that assumes a corkscrew shape when retracted, greatly expanding the surface areas to entrap fibrous material. The device is 80 cm in length and is available in 4F-6F diameters.
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