Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Integra Hallu-Fix cannulated screw driver (model number P/N 129733ND) and Recalled by Integra LifeSciences Corp. Due to The firm has received numerous complaints of 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 Integra LifeSciences Corp. directly.
Affected Products
Integra Hallu-Fix cannulated screw driver (model number P/N 129733ND) and cannulated screwdriver tip (model number P/N 129735ND). Indicated for use in fixation of fractures, osteotomies and arthrodesis of the first metatarso-phalangeal joint.
Quantity: 154 screwdrivers were distributed; 67 screwdriver tips were distributed.
Why Was This Recalled?
The firm has received numerous complaints of the cannulated screw driver tip breaking during surgery.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Integra LifeSciences Corp.
Integra LifeSciences Corp. has 216 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report