FDA today announced that Percussionaire’s recall of certain Phasitron 5 breathing circuits has been identified as Class I. The device was recalled due to the unexpected presence of nickel which could ...
FDA recently identified Sentec/Percussionaire’s correction of its Intrapulmonary Percussive Ventilation (IPV) Phasitron 5 in-line valve as Class I after the company uncovered the potential of ...
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