Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

CTL Medical Hex Driver Recalled by CTL Medical Corporation Due to the anti-toggle ring of the hex driver may...

Date: July 5, 2018
Company: CTL Medical Corporation
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 CTL Medical Corporation directly.

Affected Products

CTL Medical Hex Driver, 1/4" Square QC, 4.0 Ratcheting Ref 015.7050

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.

Related Recalls

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