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Pyxis Pro MedStation
CAREFUSION 303, INC. · Model 177-182 · UDI-DI 10885403528958
5
510(k) clearances
103,366
Adverse events (12 deaths)
99
Recalls
58
Facilities
Description
Pyxis Pro MedStation Dispensing System cabinet, table and tray, anesthesia
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-04-30 | CareFusion 303, Inc. | Fingerprint scanner may overheat to a temperature to cause 1st degree burn. |
| 2026-04-30 | CareFusion 303, Inc. | Fingerprint scanner may overheat to a temperature to cause 1st degree burn. |
| 2026-04-30 | CareFusion 303, Inc. | Fingerprint scanner may overheat to a temperature to cause 1st degree burn. |
| 2026-04-30 | CareFusion 303, Inc. | Fingerprint scanner may overheat to a temperature to cause 1st degree burn. |
| 2026-04-30 | CareFusion 303, Inc. | Fingerprint scanner may overheat to a temperature to cause 1st degree burn. |
| 2026-04-30 | CareFusion 303, Inc. | Fingerprint scanner may overheat to a temperature to cause 1st degree burn. |
| 2026-04-30 | CareFusion 303, Inc. | Fingerprint scanner may overheat to a temperature to cause 1st degree burn. |
| 2026-04-30 | CareFusion 303, Inc. | Fingerprint scanner may overheat to a temperature to cause 1st degree burn. |
| 2025-12-03 | CareFusion 303, Inc. | Due a software issue that may result in equipment not receiving timely updates of patient, medication, or related information from enterprise systems. |
| 2025-11-20 | CareFusion 303, Inc. | Automated Dispensing Cabinets (ADC) received a Half Height CUBIE drawer firmware update, which caused a Cubie Insert event which prompts software to generate a duplicate address, w |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.