Class I
Medical Device Recall: Distal Phasitron, Part: S20020, for use with Percussionaire VDR-4 control driver (or control unit)
Percussionaire Corporation · March 28, 2023
Reason for Recall
Breathing circuit reservoir bag may be assembled at the wrong attachment point, which will result in less than optimal therapy.
Distribution
US: RI, CA, TX
States Affected
CA, RI, TX
Quantity Affected
195
Source: FDA (openFDA Device Enforcement)
Recall number: Z-0693-2024
Status: ongoing
SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.