Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

Streamline MIS Navigation System Taps Recalled by RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.) Due to The Streamline MIS Navigation System taps are not...

Date: September 11, 2020
Company: RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.) directly.

Affected Products

Streamline MIS Navigation System Taps, Catalog numbers 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

Quantity: 143 units

Why Was This Recalled?

The Streamline MIS Navigation System taps are not compatible with the Streamline MIS tap sleeve.

Where Was This Sold?

Product distributed to Surgalign, a distributor located in Michigan.

About RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)

RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.) has 50 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report