--- title: "BD Pyxis MedStation ES AUX, REF 324 — FDA record Z-0972-2025 | 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-0972-2025-bd-pyxis-medstation-es-aux-ref-324/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement # BD Pyxis MedStation ES AUX, REF 324 — FDA record Z-0972-2025 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 ES AUX, REF 324 - **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**: 39615 units - **Agency-reported status**: Ongoing - **Source record identifier**: Z-0972-2025 [Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0972-2025%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 10885403512681, Serial Numbers: 9418071, 9418110, 9418124, 9525533, 9525534, 9525559, 9525563, 9525583, 9525601, 9525603, 9525604, 9525607, 9525614, 9525615, 9525616, 9525617, 9525618, 9525629, 9526868, 9528856, 9528857, 9528924, 9528931, 9529144, 9529535, 9530924, 9531251, 9531255, 9531258, 9632432, 9632438, 9632452, 12440840, 12440841, 12448207, 12448208, 12452252, 12452264, 12455476, 12457600, 12457601, 12462734, 12462735, 12463676, 12468607, 12468608, 12468609, 12468610, 12468611, 12468612, 12468670, 12468671, 12468672, 12468673, 12468674, 12473807, 12473808, 12473809, 12473810, 12473811, 12473812, 12473813, 12473815, 12473816, 12473817, 12473887, 12473921, 12473922, 12474012, 12474013, 12474014, 12474015, 12474022, 12474071, 12476548, 12483261, 12483264, 12495456, 12498513, 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[Read the complete list at the official source](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0972-2025%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-0972-2025%22) ## Related records [Medical devices records](https://isitonrecall.com/category/medical-devices/) [CareFusion 303, Inc. records](https://isitonrecall.com/brand/carefusion-303-inc/)