Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
CTL Medical Hex Driver MIS Recalled by CTL Medical Corporation Due to the anti-toggle ring of the hex driver may...
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 CTL Medical Corporation directly.
Affected Products
CTL Medical Hex Driver MIS, 1/4" Square QC, 4.0 Ratcheting Ref 019.7050
Quantity: 133 total devices
Why Was This Recalled?
the anti-toggle ring of the hex driver may separate from the driver shaft. If this occurs during surgery, the anti-toggle ring can be pressed into the pedicle screw head and cause separation of the screw from the housing upon tightening. if the anti-toggle ring remains in the pedicle crew head and can interfere with final tightening of the pedicle screw construct. this can lead to failure of the set crew and relies of the rod from the construct.
Where Was This Sold?
distributor and user level
About CTL Medical Corporation
CTL Medical Corporation has 6 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report