PlainRecalls
FDA Devices Moderate Class II Terminated

RTI Surgical Streamline Occipito-Cervico-Thoracic (OCT) Final Driver, Common Name: Screw Driver

Reported: April 20, 2016 Initiated: March 18, 2016 #Z-1393-2016

Product Description

RTI Surgical Streamline Occipito-Cervico-Thoracic (OCT) Final Driver, Common Name: Screw Driver

Reason for Recall

Multiple lots of the 26-FNLDRIVER, may have reduced mechanical strength, resulting in driver tip fracturing during use.

Details

Units Affected
N/A
Distribution
Domestic: AL, CO, CT, FL, IN, ID, IL, MI, MS, MO, NC, NY, TX Foreign: None VA/DOD: None
Location
Marquette, MI

Frequently Asked Questions

What product was recalled?
RTI Surgical Streamline Occipito-Cervico-Thoracic (OCT) Final Driver, Common Name: Screw Driver. Recalled by RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.). Units affected: N/A.
Why was this product recalled?
Multiple lots of the 26-FNLDRIVER, may have reduced mechanical strength, resulting in driver tip fracturing during use.
Which agency issued this recall?
This recall was issued by the FDA Devices on April 20, 2016. Severity: Moderate. Recall number: Z-1393-2016.