Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
IDEV Technologies SUPERA VERITAS Interwoven Self-Expanding Nitinol Stent Transhepatic Biliary Recalled by IDEV Technologies, Inc. Due to There was an error on the outer labeling...
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 IDEV Technologies, Inc. directly.
Affected Products
IDEV Technologies SUPERA VERITAS Interwoven Self-Expanding Nitinol Stent Transhepatic Biliary System. Indicated for palliative treatment of biliary strictures produced by malignant neoplasms
Quantity: 3
Why Was This Recalled?
There was an error on the outer labeling of this device. The inner label was correct.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About IDEV Technologies, Inc.
IDEV Technologies, Inc. has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report