Camlog Usa: Medical Device Recall in 2013 - (Recall #: Z-2204-2013)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2013.

Data Source: FDA.

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.

Product Classification:

Class II

Date Initiated: August 28, 2013

Date Posted: September 25, 2013

Recall Number: Z-2204-2013

Event ID: 66143

Reason for Recall:

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

Status: Terminated

Product Quantity: 1 in USA

Code Information:

39437

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated