# FDA recall Z-0299-2021

> **RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)** · Class II · device recall initiated 2020-09-24.

## Product

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.

## Reason for recall

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

## Distribution

US Nationwide distribution including in the state of Michigan.

## Key facts

- **Recall number:** Z-0299-2021
- **Recalling firm:** RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-09-24
- **Report date:** 2020-11-04
- **Termination date:** 2024-09-16

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Marquette, MI, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0299-2021

## Citation

> AI Analytics. FDA recall Z-0299-2021. Retrieved 2026-07-11 from https://api.ai-analytics.org/recall/Z-0299-2021. Source: US FDA. Licensed CC0.

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