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

Recall Z-2421-2025 — Brand Name: Atlantis IO FLO-S Product Name: Atlantis IO FLO-S Kit Model/Catalog Number: A04B / 68020033 Software Version: n/a Product Description: The Atlantis intraoral feature locating object for suprastructures (IO FLO-S) is intended to support the prosthetic procedure with the aim of restori

U.S. FDA — Device Enforcement · United States · 2025-07-24 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2421-2025
Date of alert
2025-07-24
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Dentsply IH, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
68020033
Reported risk: The defect in the thread area will not allow the device to fully engage with an implant or analog (implant replica used for prosthetic modeling). The threads will only engage approximately 2 rotations as opposed to full engagement which is approximately 5 rotations. This equates to approximately 1mm difference in depth of engagement.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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