CareFusion 303 Recalls

5 recalls found for CareFusion 303. Check if any of your products are affected.

HIGHFDA DEVICE

CareFusion 303 BD Alaris System with Guardrails Suite MX Recall Impacts 1,025,567 Units (2026)

CareFusion 303 recalled 1,025,567 units of the BD Alaris System with Guardrails Suite MX with Point of Care Unit worldwide. The recall concerns labeling that fails to indicate which TLS version must be enabled for secure hospital Wi-Fi communication. Hospitals and clinicians should stop using the device immediately and follow manufacturer instructions. The recall was issued by the FDA and is being

CareFusion 303
Due to
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HIGHFDA DEVICE

CareFusion 303 Recalls Automated Dispensing Cabinets Due to Error Risk

CareFusion 303 recalled 53,669 units of Automated Dispensing Cabinets on November 20, 2025. A firmware update caused drawer failures, leading to potential delays in accessing medications. This recall affects devices distributed worldwide, including all U.S. states and several countries.

CareFusion 303
Automated Dispensing
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HIGHFDA DEVICE

CareFusion Recalls BD Alaris Pump Module Over Connectivity Issues

CareFusion 303 recalled 189 BD Alaris Pump Modules on November 6, 2025. The recall affects connectivity to hospital networks due to daylight savings time adjustments. Users should stop using the device immediately and follow manufacturer instructions.

CareFusion 303
Due to
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HIGHFDA DEVICE

CareFusion 303 Recalls Infusion Pump Sets Due to Performance Issues

CareFusion 303 recalled Alaris Pump Infusion Sets on September 11, 2025, after identifying performance issues. The recall affects multiple model numbers due to potential inaccuracies in flow rate and alarm settings. Healthcare providers must stop using these devices immediately and follow recall instructions.

CareFusion 303
Infusion pump
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Brand Statistics

Total Recalls
5
Pages
1