Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
RTI Surgical Streamline Occipito-Cervico-Thoracic (OCT) Final Driver Recalled by RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.) Due to Multiple lots of the 26-FNLDRIVER, may have reduced...
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 RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.) directly.
Affected Products
RTI Surgical Streamline Occipito-Cervico-Thoracic (OCT) Final Driver, Common Name: Screw Driver
Quantity: N/A
Why Was This Recalled?
Multiple lots of the 26-FNLDRIVER, may have reduced mechanical strength, resulting in driver tip fracturing during use.
Where Was This Sold?
This product was distributed to 14 states: AL, CO, CT, FL, ID, IL, IN, MI, MS, MO, NY, NC, TX, VA
About RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)
RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.) has 50 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report