Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Denali Filter-Jugular/Subclavian Delivery System Product Code: DL900J/DL950J Recalled by Bard Peripheral Vascular Inc Due to Bard Peripheral Vascular, Inc. is recalling Denali Filter-Jugular/Subclavian...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Bard Peripheral Vascular Inc directly.
Affected Products
Denali Filter-Jugular/Subclavian Delivery System Product Code: DL900J/DL950J; Indicated for use in the prevention of recurrent pulmonary embolism via placement in the vena cava.
Quantity: 2904
Why Was This Recalled?
Bard Peripheral Vascular, Inc. is recalling Denali Filter-Jugular/Subclavian Delivery System and Denali Filter-Femoral Delivery System because of the stop cocks potentially cracking.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Bard Peripheral Vascular Inc
Bard Peripheral Vascular Inc has 136 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report