FDA Device recall Z-1050-2025
BD Pyxis MedStation ES AUX Tower REF 343 BD Pyxis " MedStation 4000 AUX Tower REF 314 The BD Pyxis" MedStation ES and Pyxis" MedStation 400…
- FDA Device
- Class II
- ongoing
- Published 2025-02-05
On 2025-02-05 the FDA classified a Class II recall of BD Pyxis MedStation ES AUX Tower REF 343 BD Pyxis " MedStation 4000 AUX Tower REF 314 The BD Pyxis" MedStation ES and Pyxis" MedStation 400… by Carefusion 303, citing due to an increase in complaints of door latch assembly failures that may cause the doors to be left in an open state potentially causing inventory discrepancies, a delay in acces….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1050-2025 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-02-14 |
| Published | 2025-02-05 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Carefusion 303 |
| Distribution | AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY |
Product
BD Pyxis MedStation ES AUX Tower REF 343 BD Pyxis " MedStation 4000 AUX Tower REF 314 The BD Pyxis" MedStation ES and Pyxis" MedStation 4000 are automated dispensing cabinets (ADC) that are intended to securely store and dispense medications to a qualified and authorized healthcare provider.
Reason
Due to an increase in complaints of door latch assembly failures that may cause the doors to be left in an open state potentially causing inventory discrepancies, a delay in access to medication and/or diversion of medication.
Identifiers
| code_info | BD Pyxis MedStation ES AUX Tower Catalog Number: 343 UDI-DI code: 10885403512698 Serial Number/Equipment Number: 145359…BD Pyxis MedStation ES AUX Tower Catalog Number: 343 UDI-DI code: 10885403512698 Serial Number/Equipment Number: 14535900 14535900 14535901 14535901 14535902 14535902 14535903 14535903 14535904 14535904 14535905 14535905 14535906 14535906 14535907 14535907 14535908 14535908 14535910 14535910 14535912 14535912 14535913 14535913 14535916 14535916 14535919 14535919 14535922 14535922 14535924 14535924 14535926 14535926 14535928 14535928 14535930 14535930 14535932 14535932 14535934 14535934 14535936 14535936 14535937 14535937 14535939 14535939 14535941 14535941 14535943 14535943 14535945 14535945 14535947 14535947 14535949 14535949 14535951 14535951 14535953 14535953 14535954 14535954 14535956 14535956 14535958 14535958 14535960 14535960 14535962 14535962 14535964 14535964 14535966 14535966 14549572 14549572 14549573 14549573 14549574 14549574 14549575 14549575 14549576 14549576 14549577 14549577 14651270 14651270 14651271 14651271 14651282 14651282 14651297 14651297 14651298 14651298 14651 |
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Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1050-2025%22
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