Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Iconix Knotless 1.4mm Anchor with XBraid S (Blue/Black) REF 3911-714-520 Recalled by Riverpoint Medical, LLC Due to Use of a 1.4 drill in hard bone...
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 Riverpoint Medical, LLC directly.
Affected Products
Iconix Knotless 1.4mm Anchor with XBraid S (Blue/Black) REF 3911-714-520 Iconix Knotless 1.4mm Anchor with XBraid S (Black/White) REF 3911-714-521 The Iconix Knotless anchors are intended to be used for soft-tissue to bone fixation in the foot, ankle, knee, hip, hand, wrist, elbow and shoulder.
Quantity: 999 devices
Why Was This Recalled?
Use of a 1.4 drill in hard bone conditions caused increased insertion forces leading to subsequent failures of the inserter, when the inserters bend, it may also move off the drill hole location leading to damage of the suture construct during insertion. Suture damage may lead to suture breaks during use.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Riverpoint Medical, LLC
Riverpoint Medical, LLC has 47 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report