Product Wiki · Recalls · U.S. FDA — Device Enforcement

RTI Surgical Streamline Occipito-Cervico-Thoracic (OCT) Final Driver, Common Name: Screw Driver — recall Z-1393-2016

U.S. FDA — Device Enforcement · United States · 2016-03-18 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1393-2016
Date of alert
2016-03-18
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)
Product category
device
Product type
Devices
Reported risk: Multiple lots of the 26-FNLDRIVER, may have reduced mechanical strength, resulting in driver tip fracturing during use.
Primary source: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?start_search=1&

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