Aug

2024

FDA Recall: Software Issue Leads to Incorrect Label being Printed

Allison Pate

News

fda, recall

Company: CareFusion 303, Inc.
Date of Enforcement Report: 8/30/2024
Class II

PRODUCT

BD Pyxis QFill Replenishment Station, REF: 138904-01

Recall Number:

Z-2947-2024

REASON:

Due to software issue, their is a potential when a restock label is printed for a medication stored in a non-CUBIE location, the incorrect bin for the medication is printed on the label.

RECALLING FIRM/MANUFACTURER:

CareFusion 303, Inc.

VOLUME OF PRODUCT IN COMMERCE:

3 units

DISTRIBUTION:

US Nationwide distribution in the states of CA, FL, KS, MN, NJ, NY, PA.

About the author

Allison Pate

Allison joined SoftwareCPR in 2022, bringing along over ten years of passion for building teamwork and growth in organizations. This is established in part by the greatest University the South has to offer- Mississippi State.

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FDA Recall: Software Issue Leads to Incorrect Label being Printed

Allison Pate

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