RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.): Medical Device Recall in 2016 - (Recall #: Z-1393-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: March 18, 2016

Date Posted: April 20, 2016

Recall Number: Z-1393-2016

Event ID: 73659

Reason for Recall:

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

Status: Terminated

Product Quantity: N/A

Code Information:

26-FNLDRIVER, Lot Numbers: 177091, 177093, 183817, 207727, 223926, 227291, 229134, 230523, 232262, 233074, 234205

Distribution Pattern:

Domestic: AL, CO, CT, FL, IN, ID, IL, MI, MS, MO, NC, NY, TX Foreign: None VA/DOD: None

Voluntary or Mandated:

Voluntary: Firm initiated