Class I
Medical Device Recall: High Frequency Transport Phasitron Breathing Circuit Kit REF: A50605-D, Rx Only, CE 0123
Percussionaire Corporation · December 12, 2023
Reason for Recall
Due to an assembly error within the breathing circuit, their pressure output of the breathing circuit kit can be affected and have severe impact to the end user
Distribution
US:AL AR CA CT FL GA IL IN KS LA MI MN MO NC NJ OH OR TN TX UT VA OUS: None
States Affected
AL, AR, CA, CT, FL, GA, IL, IN, KS, LA, MI, MN, MO, NC, NJ, OH, OR, TN, TX, UT, VA
Quantity Affected
2145 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-0637-2024
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.