RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.): Medical Device Recall in 2020 - (Recall #: Z-0299-2021)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

Streamline MIS Navigation System Taps, Catalog Nos. 04-CANNDRILL-MDN 04-CANNTAP-40-MDN 04-CANNTAP-45-MDN 04-CANNTAP-55-MDN 04-CANNTAP-65-MDN 04-CANNTAP-75-MDN 04-CANNTAP-85-MDN 04-CTAP-TT-65-MDN 04-S-FINDER-MDN 05-SCREWINS-CL-MDN 05-SIMPDRIVER-MDN Product Usage: intended to be used during the preparation and placement of screws from the Streamline TL and MIS Systems and preparation of screws from the Streamline OCT System during spinal surgery to assist the surgeon in precisely locating anatomical structures in either open or minimally invasive procedures.

Product Classification:

Class II

Date Initiated: September 24, 2020

Date Posted: November 4, 2020

Recall Number: Z-0299-2021

Event ID: 86559

Reason for Recall:

The Streamline Navigation System taps have experienced binding with other devices.

Status: Terminated

Product Quantity: 420 units

Code Information:

Lots 377520 371734 374791 374792 373438 371735 371736 377625 377806 371737 372819 371266 371733

Distribution Pattern:

US Nationwide distribution including in the state of Michigan.

Voluntary or Mandated:

Voluntary: Firm initiated