CareFusion 303, Inc.: BD Pyxis MedStation ES Cabinets Recalled for Door and Drawer Failures

What You Should Do

1. Identify if your facility is using affected BD Pyxis MedStation models by checking the serial numbers against the extensive list provided in the recall notice.
2. Specifically, check for BD Pyxis MedStation ES (REF: 323), BD Pyxis MedStation Auxiliary ES (REF: 324), BD Pyxis MedStation Auxiliary 4000 (REF: 306), and BD Pyxis MedStation 4000 (REF: 303).
3. Verify the UDI numbers for affected units: 0885403212667 (Med ES Main), 10885403512681 (Auxiliary ES), 10885403512636 (Auxiliary 4000), and 10885403512629 (MedStation 4000).
4. Contact the manufacturer, CareFusion 303, Inc., or your healthcare provider for guidance on how to address mechanical failures and for information on potential repairs or refunds.
5. Report any adverse events or quality problems experienced with the use of this product to the FDA's MedWatch Adverse Event Reporting program at 1-800-FDA-1088 or online at www.fda.gov/medwatch.
6. For additional questions regarding this recall, contact the FDA at 1-888-463-6332.

Your Remedy Options

Affected Products