Medical Device Safety and Recalls: Teleflex Hudson RCI Lifesaver Single Patient Use Manual Resuscitator Intake Port Blockage

["U.S. Food & Drug Administration (FDA)" <fda@xxxxxxxxxxxxxxxxxxxxxxx>]

Title: Medical Device Safety and Recalls: Teleflex Hudson RCI Lifesaver Single Patient Use Manual Resuscitator Intake Port Blockage

A recall has been issued for the Teleflex Hudson RCI Lifesaver Single Patient Use Manual Resuscitator.  The oxygen intake port may be blocked which can prevent the bag from filling. This may prevent the device from delivering breathing support to the patient. A delay in treatment may potentially lead to patient injury or death. To date, Teleflex has not received any reports of patient injury or death related to this recall.

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