Home / Recalls / Camlog Usa / Z-2204-2013

Z-2204-2013 Class II Terminated

Recalled by Camlog Usa — Indianapolis, IN

Recall Details

Product Type
Devices
Report Date
September 25, 2013
Initiation Date
August 28, 2013
Termination Date
January 29, 2014
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
1 in USA

Product Description

C2244.3820;, CONELOG Titanium Base CC ¿3.8GH2.0 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.

Reason for Recall

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

Distribution Pattern

USA Distribution in the states of NH, MD, CO, and IL.

Code Information

39437

Other recalls by Camlog Usa

  • Z-2205-2013 Class II — C2244.4308 CONELOG Titanium Base CC ¿4.3GH2 0.8 inkl HS Product Usage: Endos (August 28, 2013)
  • Z-2203-2013 Class II — C2244.3808, CONELOG Titanium Base CC ¿3.8GH0.8 inkl HS Product Usage: Endoss (August 28, 2013)
  • Z-2206-2013 Class II — C2244.5008 CONELOG Titanbasis CAD/CAM Conelog Titanium Base CAD/CAM Rx only (August 28, 2013)