Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
VenaSeal Closure System Recalled by Medtronic Inc. Due to Firm received increased number of reports that VenaSeal...
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 Medtronic Inc. directly.
Affected Products
VenaSeal Closure System
Quantity: 154,152 units
Why Was This Recalled?
Firm received increased number of reports that VenaSeal dispensing systems are not effectively advancing the adhesive forward through the delivery catheter.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Medtronic Inc.
Medtronic Inc. has 85 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report