FDA recall record

Cook Medical Gunther Tulip Vena Cava Filter Set for Femoral and Jugular Vein Approach recall — FDA Z-1023-2019

Updates to the Instructions for Use.

Class IIIclassification
Z-1023-2019official record ID
Mar 27, 2019report date

Recall record at a glance

Official recordZ-1023-2019
CategoryMedical Device Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmCook Medical Inc.
Report dateMar 27, 2019
Recall initiation dateFeb 25, 2019
Quantity91731 total
LocationBloomington, IN, United States

Official product description

Gunther Tulip Vena Cava Filter Set for Femoral and Jugular Vein Approach, Catalog Number IGTCFS-65-1-UNl-TULIP Product Usage: The Gunther Tulip Filter is intended for the prevention of recurrent pulmonary embolism (PE) via placement in the vena cava in the following situations:(1) Pulmonary thromboembolism when anticoagulant therapy is contraindicated; (2) Failure of anticoagulant therapy in thromboembolic diseases; (3) Emergency treatment following massive PE where anticipated benefits of conventional therapy are reduced; and (4) Chronic, recurrent PE where anticoagulant therapy has failed or is contraindicated. The Filter implant may be retrieved if clinically indicated. The product is intended for percutaneous placement via a femoral or jugular vein for filtration of inferior vena cava (IVC) blood to prevent PE.

Why the product was recalled

Updates to the Instructions for Use.

Distribution information

The products were distributed US Nationwide Distribution

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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