Product Wiki · Recalls · U.S. FDA — Device Enforcement

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-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

U.S. FDA — Device Enforcement · United States · 2020-09-11 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0320-2021
Date of alert
2020-09-11
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)
Product category
device
Product type
Devices
Reported risk: The Streamline MIS Navigation System taps are not compatible with the Streamline MIS tap sleeve.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.