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Camlog Usa recalls C2244.3808, CONELOG Titanium Base CC ¿3.8GH0.8 inkl HS Product Usage: Endosseous dental implant abutment CONELOG Abu
Recalled September 25, 2013 · FDA recall Z-2203-2013 · Camlog Usa
Hazard
Product not cleared for sale/use in the United States. · FDA Class II
Units
2 in USA
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
C2244.3808, CONELOG Titanium Base CC ¿3.8GH0.8 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 →