FDA Recall Terminated

CareStream Dental Kodak 2200 Intraoral X-ray system Product Usage: The expected usage (intended use) for all of these products is for dental radiographic examination and diagnosis of the teeth, jaw and oral structures.

Recall: Z-1095-2013 · Initiated September 18, 2012

Recall

Recall Number
Z-1095-2013
Event Number
64589
Firm
Trophy Sas 4 Rue Pelloutier Croissy Beaubourg France
FEI Number
7695
Product Code
EAP
Status
Terminated
Root Cause
Radiation Control for Health and Safety Act
Initiated
September 18, 2012
Posted
May 2, 2013
Terminated
May 2, 2017

Description

CareStream Dental Kodak 2200 Intraoral X-ray system Product Usage: The expected usage (intended use) for all of these products is for dental radiographic examination and diagnosis of the teeth, jaw and oral structures.

Reason

There have been approximately 2% of the x-ray generators manufactured between February 2012 and November 2012 returned due to errors. These generators showed the type of defect that indicates poor contact of HT transformer power pin. The defect is a bent connector associated with the generator.

Action

Trophy, A Carestream Dental Company, - A Subsidiary of Carestream Health Inc. The Center for Devices (CDRH) understands that the corrective action plan (CAP) involving 167 units will consist of implementing rework procedure TL008, which describes the procedure for a bending the metallic strip the female connector to insure strong connection with the male counterpart. The CAP appears to adequately address the problem and is hereby approved For further questions please call (585) 781-1997.

Distribution

USA Nationwide Distribution

Quantity

167 installed in the US