CareFusion 303, Inc.: BD Pyxis Automated Dispensing Cabinets Recalled for Electrical Shock Risk

What You Should Do

1. Identify if your facility is using BD Pyxis MedBank Mini or Tower systems by checking the REF/Model numbers on the device or the UDI-DI codes 10885403512544 or 10885403512568.
2. Check the manufacturing date of the equipment to see if it falls between November 15, 2012, and July 25, 2023.
3. Verify if you are using the updated User Guide versions for your specific model: BD Pyxis CUBIE Replenishment Station (DIR 10000414989), MedBank Cabinet (DIR 10000414987), or MedBank Installation and Upgrade Guide (DIR 10000414990).
4. Contact CareFusion 303, Inc. at their San Diego headquarters (10020 Pacific Mesa Blvd, San Diego, CA 92121) or through your established BD service representative to discuss the status of your power strips and necessary safety updates.
5. If you have questions about the safety of the medical device, contact your healthcare provider or the manufacturer directly.
6. For additional information, you may contact the FDA at 1-888-463-6332 (1-888-INFO-FDA) or visit www.fda.gov/medical-devices/medical-device-recalls.

Your Remedy Options

Affected Products