RecallRadar

FDA Device recall Z-0299-2021

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-MD…

On 2020-11-04 the FDA classified a Class II recall of 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-MD… by Rti Surgical Dba Pioneer Surgical Technology, citing the Streamline Navigation System taps have experienced binding with other devices.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-0299-2021
ClassificationClass II
Statusterminated
Initiated2020-09-24
Published2020-11-04
Last updated2026-09-13 11:55 UTC
CompanyRti Surgical Dba Pioneer Surgical Technology
DistributionUS

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

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

Identifiers

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

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0299-2021%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.