Z-2947-2024 Class II Ongoing
FDA device recall Z-2947-2024 was initiated by CareFusion 303, Inc. on July 9, 2024 and is designated Class II. Reason for recall: Due to software issue, there is a potential when a restock label is printed for a medication stored in a non-CUBIE location, that the incorrect bin for the medication is printed on the label. The recall status is ongoing. Affected quantity: 3 units.
Recall Details
- Product Type
- Devices
- Report Date
- September 11, 2024
- Initiation Date
- July 9, 2024
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 3 units
Product Description
BD Pyxis QFill Replenishment Station, REF: 138904-01, medication cabinet system
Reason for Recall
Due to software issue, there is a potential when a restock label is printed for a medication stored in a non-CUBIE location, that the incorrect bin for the medication is printed on the label.
Distribution Pattern
US Nationwide distribution in the states of CA, FL, KS, MN, NJ, NY, PA.
Code Information
serial numbers: 44210411, 43880801, 44227426/ UDI: None