Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Barricaid Annual Closure Device (ACD) BAR-A8-8MM - Product Usage: The Recalled by Intrinsic Therapeutics, Inc. Due to The catalog ( REF ) number on the...
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 Intrinsic Therapeutics, Inc. directly.
Affected Products
Barricaid Annual Closure Device (ACD) BAR-A8-8MM - Product Usage: The Barricaid¿ ACD is indicated for reducing the incidence of reherniation, and reoperation in skeletally mature patients with radiculopathy (with or without back pain) attributed to a posterior or posterolateral herniation, and confirmed by history, physical examination and imaging studies which demonstrate neural compression using MRI to treat a large annular defect (between 4-6 mm tall and between 6-10 mm wide) following a primary discectomy procedure (excision of herniated intervertebral disc) at a single level between L4 and S1.
Quantity: 110 units
Why Was This Recalled?
The catalog ( REF ) number on the peelable inner labels (patient sticker) that is on the inner container (box) is incorrect. It states BAR-A8-10MM instead of BAR-A8-8MM.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Intrinsic Therapeutics, Inc.
Intrinsic Therapeutics, Inc. has 2 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report