--- title: "BD Pyxis MedStation 4000 AUX, REF 306 — FDA record Z-0974-2025 | Is It on Recall" description: "Drawer and/or door failures that may lead to a delay in access to medications. The following three situations in which drawer and/or door failures may occur hav" url: https://isitonrecall.com/recall/fda-device-z-0974-2025-bd-pyxis-medstation-4000-aux-ref-306/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement # BD Pyxis MedStation 4000 AUX, REF 306 — FDA record Z-0974-2025 Reported ongoing Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice. Source date Feb 14, 2023. Retrieved Oct 1, 2026. Last updated Oct 1, 2026. Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/). ## What the record says - **Product**: BD Pyxis MedStation 4000 AUX, REF 306 - **Reason**: Drawer and/or door failures that may lead to a delay in access to medications. The following three situations in which drawer and/or door failures may occur have been identified: Situation 1: Door Latch Failure, Situation 2: Cable Ribbon Damage, Situation 3: Magnet Falling Out, - **Classification**: Class II - **Recalling firm**: CareFusion 303, Inc. - **Quantity**: 5056 units - **Agency-reported status**: Ongoing - **Source record identifier**: Z-0974-2025 [Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0974-2025%22) [What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice. ## Lot and product identifiers | Label field | Details supplied by the agency | | --- | --- | | Lot, code or applicability | UDI/DI 10885403512636, Serial Numbers: 9304700, 9305723, 9309302, 9413001, 9413014, 9415602, 9415665, 9417311, 9417312, 9417335, 9417340, 9417428, 9417430, 9417433, 9417437, 9418065, 9418068, 9418100, 9418105, 9418111, 9418112, 9418113, 9418114, 9418115, 9418129, 9418568, 9523679, 9525535, 9525558, 9525560, 9525561, 9525562, 9525582, 9525590, 9525600, 9525605, 9525606, 9525613, 9525624, 9525630, 9525638, 9525656, 9525657, 9526867, 9528530, 9528836, 9528859, 9528890, 9531253, 9531257, 12439518, 12439520, 12439521, 12439907, 12440208, 12440217, 12440218, 12440219, 12440220, 12440227, 12440339, 12440984, 12440985, 12443922, 12443923, 12445433, 12447385, 12447387, 12447388, 12447389, 12447394, 12447395, 12447396, 12448203, 12448204, 12452249, 12452265, 12452646, 12452649, 12453000, 12453215, 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[Read the complete list at the official source](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0974-2025%22). Match all identifying details in the current notice. A brand name alone is not enough. ## Distribution Worldwide No US distribution state could be established from this record. Check the official notice. ## Dates in the source - **Report date**: Jan 29, 2025 - **Recall initiation date**: Feb 14, 2023 - **Center classification date**: Jan 17, 2025 FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable. ## What to do next Read the official notice for the action that applies to your exact product. [Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0974-2025%22) ## Related records [Medical devices records](https://isitonrecall.com/category/medical-devices/) [CareFusion 303, Inc. records](https://isitonrecall.com/brand/carefusion-303-inc/)