Company: Moog, Inc.Date of Enforcement Report 4/8/2011 Class l: Moog Incannounced today that the Food and Drug Administration (FDA) has classified the voluntary correction of the Curlin 6000 CMS, Curlin 6000 CMS IOD, PainSmart, and PainSmart IOD as a Class I recall. The affected models were manufactured and updated from May 2007 to February 2011....Read More