CareFusion 303, Inc.
CareFusion 303, Inc.: 4 recalls listed since January 2026 across FDA.
By year
- 20264
By agency
- FDA4
By category
- Medical Device4
All recalls (4)
CareFusion 303 BD Pyxis Medication Cabinets
BD Pyxis medication cabinets have a fingerprint scanner that may overheat and cause first-degree burns.
8 products
BD Alaris System with Guardrails Suite MX with Point of Care Unit
The BD Alaris System with Guardrails Suite MX with Point of Care Unit lacks labeling for secure Wi-Fi communication.
BD Alaris Pump Module Model 8100
The BD Alaris Pump Module may have a date and time issue causing connectivity problems with hospital networks.
BD Pyxis ES Enterprise Server
BD Pyxis ES Enterprise Server has a software issue that may result in equipment not receiving timely updates of patient, medication, or related information.