Teleflex (NYSE:TFX) is recalling its Hudson RCI Lifesaver single patient use manual resuscitator, according to an FDA posting.
The Wayne, Penn.-based company began notifying customers of the issue on May 14.
The FDA has labeled the recall as a Class I, the most serious type of recall issued by the federal watchdog, which indicates “there is a reasonable probability that use of these products will cause serious adverse health consequences or death.”
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