Moog Infusion Pumps Face Class I Recall

Law360, New York (April 13, 2011, 1:47 PM EDT) -- Moog Inc. announced Friday that the U.S. Food and Drug Administration had labeled the company's voluntary corrective steps over certain ambulatory infusion pumps as a Class I recall, the most serious kind.

The affected pump models in the Class I recall include the Curlin 6000 CMS, Curlin 6000 CMS IOD, PainSmart and PainSmart IOD manufactured and updated from May 2007 to February 2011, Moog said in a statement.

East Aurora, N.Y.-based Moog said the recall was sparked by a software anomaly that led to a particular...
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