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

Recall Z-2172-2025 — The Drill Stop Kit is the version of the Mini Sterilizable Tray that is used to store, sterilize, verify Drill Stop length, and facilitate the mounting/removal of the Drill Stops. The Drill Stop Kit includes the Release Bracket, which is used for mounting and removing Drill Stops, as well as verifyi

U.S. FDA — Device Enforcement · United States · 2025-05-01 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2172-2025
Date of alert: 2025-05-01
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Implant Direct Sybron Manufacturing LLC
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 15006511

Reported risk: The Drill stop kit contains incorrect components.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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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.

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