Law360, New York (September 16, 2010, 1:08 PM ET) -- WestMed Inc., a respiratory device manufacturer, has made a Class I recall of 24,384 units of its BagEasy Manual Resuscitation Devices because of reports that they can stop operating.
The products were voluntarily yanked off the market by WestMed and classified by the U.S. Food and Drug Administration under its most severe scale of product recall, where there is a potential for injury or death, according to a statement from the agency Wednesday.
WestMed recalled the products after reports from three separate facilities that units disconnected...
WestMed Issues Class I Recall Of Resuscitators
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