Medical DeviceJun 10, 2026
CareFusion 303 BD Pyxis MedBank Tower REF: 1145-00 Medication cabinet recall — FDA Z-2303-2026
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
Class IIFDA: OngoingCareFusion 303, Inc.
Recall history in this database
Classification mix: Class II: 9.
Medical DeviceJun 10, 2026
CareFusion 303 BD Pyxis Mini Main REF: 349 Medication cabinet recall — FDA Z-2301-2026
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
Class IIFDA: OngoingCareFusion 303, Inc.
Medical DeviceJun 10, 2026
CareFusion 303 BD Pyxis Anesthesia Station 4000 REF: 338 Medication cabinet recall — FDA Z-2300-2026
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
Class IIFDA: OngoingCareFusion 303, Inc.
Medical DeviceJun 10, 2026
CareFusion 303 BD Pyxis MedStation ES REF: 323 Medication cabinet recall — FDA Z-2298-2026
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
Class IIFDA: OngoingCareFusion 303, Inc.
Medical DeviceJun 10, 2026
CareFusion 303 BD Pyxis Anesthesia Station ES REF: 327 Medication cabinet recall — FDA Z-2299-2026
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
Class IIFDA: OngoingCareFusion 303, Inc.
Medical DeviceJun 10, 2026
CareFusion 303 BD Pyxis MedStation 4000 REF: 303 Medication cabinet recall — FDA Z-2297-2026
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
Class IIFDA: OngoingCareFusion 303, Inc.
Medical DeviceJun 10, 2026
CareFusion 303 BD Pyxis MedBank Mini REF: 1147-00 Medication cabinet recall — FDA Z-2304-2026
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
Class IIFDA: OngoingCareFusion 303, Inc.
Medical DeviceJun 10, 2026
CareFusion 303 BD Pyxis MedStation ES Tower REF: 352 Medication cabinet recall — FDA Z-2302-2026
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
Class IIFDA: OngoingCareFusion 303, Inc.
Medical DeviceApr 1, 2026
CareFusion 303 BD Alaris" System with Guardrails" Suite MX with Point of Care Unit recall — FDA Z-1645-2026
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
Class IIFDA: OngoingCareFusion 303, Inc.
Understanding this recall history
This page summarizes recall records in which the official source identifies CareFusion 303, Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.