Z-2948-2024 Class II Ongoing
FDA device recall Z-2948-2024 was initiated by CareFusion 303, Inc. on Jul 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.
Recall Details
- Product Type
- Devices
- Report Date
- Sep 11, 2024
- Initiation Date
- Jul 9, 2024
- Voluntary/Mandated
- Voluntary: Firm initiated
Product Description
BKIT BD Pyxis QFill Replenishment Station, REF: 155197-01, 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: 16056243 16068264 16082950 16142772 16192674 16208218 16208219 16284106 16346254 16388826 16388833 16623139 / UDI: None
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-2948-2024
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 26, 2026