CareFusion 303, Inc. recalled BD PYXIS MDBNK TWR MN CR-4HH-5FM-P RxNow automated dispensing cabinets with software version 3.9.1.9 due to a potential for incorrect medication bin labels, the FDA said on June 24, 2024.
How to tell if you have it
- BD PYXIS MDBNK TWR MN CR-4HH-5FM-P RxNow
- REF: 169-131
- Software version 3.9.1.9
- UDI: 10885403512568
- Serial Numbers: 16139674, 16124908, 16063924, 16084467, 16221549, 16139675, 16220875, 16237258, 16284001, 15940400, 15940104, 15941703, 15941654, 15943750, 15943749, 15500696, 15654711, 15654721, 15631099, 15631104, 15775749, 15383480, 15383481, 15383475, 15383486, 15383487, 15366328, 15606170, 15575974, 15575976, 15490745, 15422133, 15853047, 15902413, 15598095, 15550853, 15437809, 15437812, 15518269, 15518273, 15518270, 15872432, 15872429, 15662816, 15504833, 15504836, 15503511, 15430948, 15430963, 15639687, 15639724, 15639720, 15639718, 15328493, 15442794, 15442789, 15761398, 15761401, 15937579, 15786154, 15684803
The hazard
Due to a software issue, there is a potential that when a restock label is printed for a medication stored in automated dispensing cabinets, the incorrect bin for the medication is printed on the label.
Context
GovInfoNow's records show CareFusion 303, Inc. has 64 other recalls on record since 2017-06-12. Other recent recalls of similar products include BD Pyxis Mini Main REF 349 Medication Cabinet Recall (2026-04-30), CareFusion TLS Version Labeling Recall (2026-02-11), and BD Pyxis ES Enterprise Server Software Update Issue Recall (2025-12-03). Other recent recalls of similar products include Baxter Novum IQ Syringe Pump Recall (2026-08-11), Medtronic SynchroMed Flex Infusion Software Issue Recall (2026-04-08), and Fresenius Medical Care Bicarby Dialysate Recall (2026-05-07).