# FDA recall Z-0320-2021

> **RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)** · Class II · device recall initiated 2020-09-11.

## Product

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

## Reason for recall

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

## Distribution

Product distributed to Surgalign, a distributor located in Michigan.

## Key facts

- **Recall number:** Z-0320-2021
- **Recalling firm:** RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-09-11
- **Report date:** 2020-11-11
- **Termination date:** 2024-05-23

- **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-0320-2021

## Citation

> AI Analytics. FDA recall Z-0320-2021. Retrieved 2026-08-19 from https://api.ai-analytics.org/recall/Z-0320-2021. Source: US FDA. Licensed CC0.

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