Class II — Potential Health Hazard

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...

Date: March 18, 2016
Company: RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)
Status: Terminated
Source: FDA (Device)

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

Affected (14 states)Not affected

About RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)

RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.) has 50 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report