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
- Recalling Firm
- RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)
- 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.
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