Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0518-2024 — 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 should

U.S. FDA — Device Enforcement · United States · 2023-10-25 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0518-2024
Date of alert
2023-10-25
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Riverpoint Medical, LLC
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00840277402172
Reported risk: 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.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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