HIGH
FDA DEVICE
BD Pyxis MedStation ES REF: 323 Medication cabinet
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
CareFusion 303
Fingerprint scanner
Brand hub
CareFusion 303 Recalls
13 recalls found for CareFusion 303. Check current safety alerts and related brands before using affected products.
- Active recalls
- 13
- Pages
- 1
HIGH
FDA DEVICE
BD Pyxis MedStation ES Tower REF: 352 Medication cabinet
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
CareFusion 303
Fingerprint scanner
HIGH
FDA DEVICE
BD Pyxis MedBank Tower REF: 1145-00 Medication cabinet
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
CareFusion 303
Fingerprint scanner
HIGH
FDA DEVICE
BD Pyxis Mini Main REF: 349 Medication cabinet
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
CareFusion 303
Fingerprint scanner
HIGH
FDA DEVICE
BD Pyxis Anesthesia Station ES REF: 327 Medication cabinet
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
CareFusion 303
Fingerprint scanner
HIGH
FDA DEVICE
BD Pyxis MedStation 4000 REF: 303 Medication cabinet
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
CareFusion 303
Fingerprint scanner
HIGH
FDA DEVICE
BD Pyxis MedBank Mini REF: 1147-00 Medication cabinet
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
CareFusion 303
Fingerprint scanner
HIGH
FDA DEVICE
BD Pyxis Anesthesia Station 4000 REF: 338 Medication cabinet
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
CareFusion 303
Fingerprint scanner
Health & Personal Care
HIGH
FDA DEVICE
CareFusion 303 BD Alaris System with Guardrails Suite MX Recall Impacts 1,025,567 Units (2026)
Due to product labeling not indicating which Transport Layer Security (TLS) version that must be enabled on hospital network to ensure secure Wi-Fi communication with Point-of-Care Units
CareFusion 303
Due to
Health & Personal Care
HIGH
FDA DEVICE
CareFusion 303 Recalls Automated Dispensing Cabinets Over Software Issues
Due a software issue that may result in equipment not receiving timely updates of patient, medication, or related information from enterprise systems.
CareFusion 303
Due a
Health & Personal Care
HIGH
FDA DEVICE
CareFusion 303 Recalls Automated Dispensing Cabinets Due to Error Risk
CareFusion 303
Automated Dispensing
Health & Personal Care
HIGH
FDA 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
Health & Personal Care
HIGH
FDA DEVICE
CareFusion 303 BD Alaris Infusion Sets Recalled for Flow, Bolus Accuracy Issues (2025)
Infusion pump module used with compatible pump infusion sets may perform outside the established performance ranges for flow rate and bolus accuracy, downstream and upstream occlusion time to alarm, and post-occlusion bolos volume.
CareFusion
Infusion pump
Brand Statistics
Total Recalls
13
Pages
1