Data Foundry

Medical device recalls 2020

Streamline MIS Navigation System Taps — Class II medical device recall Z-0320-2021

Terminated recall by RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.), reported 2020-11-11, distributed in MI. The Streamline MIS Navigation System taps are not compatible with the Streamline MIS tap sleeve.

Recall numberZ-0320-2021
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmRTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.), Marquette, MI, United States
Recall initiated2020-09-11
Classified2020-10-31
Reported by FDA2020-11-11
Terminated2024-05-23
DistributedMI
Quantity143 units
Lot numbers371266, 371733, 371734, 371735, 371736, 371737, 372819, 373438, 374791, 374792, 377520, 377625, 377806
Model numbers04-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

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.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0320-2021. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.