company
CareFusion 303, Inc.
Jurisdiction: US
FDA Warning Letter timeline
V1 scope: FDA Warning Letters only. Additional public-record sources (SEC, CPSC, federal contracts) are on the V2 roadmap and are not surfaced here today.
- fda_recall · device_recall2026-06-10CareFusion 303, Inc. — Class II recall: BD Pyxis MedStation ES REF: 323 Medication cabinet
- fda_recall · device_recall2026-06-10CareFusion 303, Inc. — Class II recall: BD Pyxis Anesthesia Station 4000 REF: 338 Medication cabinet
- fda_recall · device_recall2026-06-10CareFusion 303, Inc. — Class II recall: BD Pyxis MedStation 4000 REF: 303 Medication cabinet
- fda_recall · device_recall2026-06-10CareFusion 303, Inc. — Class II recall: BD Pyxis MedStation ES Tower REF: 352 Medication cabinet
- fda_recall · device_recall2026-06-10CareFusion 303, Inc. — Class II recall: BD Pyxis Anesthesia Station ES REF: 327 Medication cabinet
- fda_recall · device_recall2026-06-10CareFusion 303, Inc. — Class II recall: BD Pyxis MedBank Mini REF: 1147-00 Medication cabinet
- fda_recall · device_recall2026-06-10CareFusion 303, Inc. — Class II recall: BD Pyxis Mini Main REF: 349 Medication cabinet
- fda_recall · device_recall2026-06-10CareFusion 303, Inc. — Class II recall: BD Pyxis MedBank Tower REF: 1145-00 Medication cabinet
Frequently asked questions
- How many FDA warning letters has CareFusion 303, Inc. received?
- Argus HQ has not recorded an FDA warning letter for CareFusion 303, Inc. in our current dataset.
- What FDA recalls has CareFusion 303, Inc. issued?
- Argus HQ has recorded 8 FDA recalls tied to CareFusion 303, Inc..
- Is CareFusion 303, Inc. FDA compliant?
- Argus HQ is not a compliance rating service. As of this page's last update, our dataset shows 0 warning letters, 8 recalls, and 0 approval records for CareFusion 303, Inc.. Review the linked FDA source records directly before drawing a compliance conclusion.
Informational only. FDA Warning Letters are public records (17 USC §105). Summaries are AI-assisted and may contain errors; always verify against the original FDA letter before acting. Not legal, financial, or regulatory advice.