--- title: "BD Pyxis MedStation 4000 Main, REF 303 — FDA record Z-0973-2025 | 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-0973-2025-bd-pyxis-medstation-4000-main-ref-303/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement # BD Pyxis MedStation 4000 Main, REF 303 — FDA record Z-0973-2025 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 Main, REF 303 - **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**: 13055 units - **Agency-reported status**: Ongoing - **Source record identifier**: Z-0973-2025 [Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0973-2025%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 10885403512629, Serial Numbers: 12439536, 12439538, 12439539, 12439540, 12439541, 12439544, 12440786, 12440787, 12440788, 12440789, 12440790, 12440791, 12440792, 12440978, 12440979, 12441431, 12443165, 12446066, 12448071, 12448072, 12448073, 12448074, 12448142, 12450907, 12450908, 12450909, 12450910, 12450911, 12450912, 12450913, 12450914, 12450915, 12450968, 12450970, 12450971, 12450973, 12450974, 12450975, 12450976, 12451251, 12451628, 12452651, 12452991, 12452993, 12453011, 12453012, 12453013, 12455427, 12455859, 12457587, 12457588, 12457589, 12457590, 12459775, 12461364, 12461365, 12461368, 12461369, 12461516, 12461517, 12461518, 12461520, 12462977, 12462978, 12463388, 12465197, 12465198, 12465199, 12465200, 12466882, 12468231, 12468628, 12470401, 12470403, 12470405, 12470879, 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[Read the complete list at the official source](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0973-2025%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-0973-2025%22) ## Related records [Medical devices records](https://isitonrecall.com/category/medical-devices/) [CareFusion 303, Inc. records](https://isitonrecall.com/brand/carefusion-303-inc/)