RecallRadar

FDA Device recall Z-0320-2021

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…

On 2020-11-11 the FDA classified a Class II recall of 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… by Rti Surgical Dba Pioneer Surgical Technology, citing the Streamline MIS Navigation System taps are not compatible with the Streamline MIS tap sleeve.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-0320-2021
ClassificationClass II
Statusterminated
Initiated2020-09-11
Published2020-11-11
Last updated2026-09-13 11:55 UTC
CompanyRti Surgical Dba Pioneer Surgical Technology
DistributionMI

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

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

Identifiers

code_infoLot numbers 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-0320-2021%22

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