Z-0906-2025 Class II Ongoing
FDA device recall Z-0906-2025 was initiated by CareFusion 303, Inc. on April 5, 2023 and is designated Class II. Reason for recall: Due to an automated dispensing cabinet software issue, when a medication single order contains more than one component and at least one is unavailable for a multi-item or combination order, the order … The recall status is ongoing. Affected quantity: 622.
Recall Details
- Product Type
- Devices
- Report Date
- January 22, 2025
- Initiation Date
- April 5, 2023
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 622
Product Description
BD Pyxis MedStation ES (Med ES Main), REF: 323; and BD Pyxis MedStation ES (Med ES Main Tower), REF: 352
Reason for Recall
Due to an automated dispensing cabinet software issue, when a medication single order contains more than one component and at least one is unavailable for a multi-item or combination order, the order may display as grayed out; alternate location tooltip will display "Server connection failed," not listing other area devices where unavailable item(s) may be found, which may lead to delayed therapy.
Distribution Pattern
US Nationwide distribution in the states of NY, NC, LA.
Code Information
Software v1.7.3. REF/UDI-DI: 323/10885403512667, 352/10885403512674