Recall Z-2947-2024— CareFusion 303, Inc.
Class II · Ongoing
Class II FDA medical device recall by CareFusion 303, Inc., initiated 2024-07-09. FDA's recall record names no specific 510(k) clearance for this event. Product: BD Pyxis QFill Replenishment Station, REF: 138904-01, medication cabinet system. Reason: 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..
- Recalling firm
- CareFusion 303, Inc.
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2024-07-09
- Firm location
- San Diego, CA, United States
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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.