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Camlog Usa recalls C2244.4308 CONELOG Titanium Base CC ¿4.3GH2 0.8 inkl HS Product Usage: Endosseous dental implant abutment CONELOG Ab
Recalled September 25, 2013 · FDA recall Z-2205-2013 · Camlog Usa
Hazard
Product not cleared for sale/use in the United States. · FDA Class II
Units
6 to US customers
Sold at
USA Distribution in the states of NH, MD, CO, and IL.
Description
Product not cleared for sale/use in the United States.
Product
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.
Manufacturer(s)
Camlog Usa
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →