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

Recall Z-2205-2013 — C2244.4308 CONELOG Titanium Base CC ¿4.3GH2 0.8 inkl HS Product Usage: Endosseous dental implant abutment CONELOG Abutments are intended to be used to fabricate prosthetic restorations in conjunction with CONELOG implants to support prostheses in the maxillary and/or mandibular arch.

U.S. FDA — Device Enforcement · United States · 2013-08-28 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2205-2013
Date of alert: 2013-08-28
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Camlog Usa
Product category: device
Product type: Devices

Reported risk: Product not cleared for sale/use in the United States.

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.

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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