Class II
Medical Device Recall: BD Pyxis QFill Replenishment Station, REF: 138904-01, medication cabinet system
CareFusion 303, Inc. · July 9, 2024
Reason for Recall
Due to software issue, there is a potential when a restock label is printed for a medication stored in a non-CUBIE location, that the incorrect bin for the medication is printed on the label.
Distribution
US Nationwide distribution in the states of CA, FL, KS, MN, NJ, NY, PA.
States Affected
NATIONWIDE
Quantity Affected
3 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-2947-2024
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.