FDA Enforcement History: CareFusion 303, Inc.

FDA action counts

Risk pattern analysis

Argus HQ analysis — not an FDA finding

This section is Argus HQ analysis, not an FDA finding. CareFusion 303, Inc. has 8 separate FDA recalls on file, more than a single isolated recall event. A pattern across multiple FDA touchpoints does not by itself establish that any specific product currently poses a risk; it reflects only the frequency of FDA engagement with this company as recorded in Argus HQ's database. Argus HQ ingests these records directly from FDA's own public enforcement and approval databases rather than from company disclosures. This page reflects only the FDA event types Argus HQ currently tracks -- FDA Warning Letters, recalls, drug and biologic approvals, and Form 483 inspection observations -- and will update automatically as new FDA records are observed. Argus HQ does not independently verify FDA's underlying findings; this page summarizes what FDA has published and links back to the original FDA source for each event.

Enforcement history

On 2026-06-10, Argus HQ recorded a FDA recall for CareFusion 303, Inc., rated "high" severity in Argus HQ's classification: CareFusion 303, Inc. — Class II recall: BD Pyxis MedBank Tower REF: 1145-00 Medication cabinet An FDA recall record reflects a firm removing or correcting a product already in distribution because it does not meet FDA requirements. On 2026-06-10, Argus HQ recorded a FDA recall for CareFusion 303, Inc., rated "high" severity in Argus HQ's classification: CareFusion 303, Inc. — Class II recall: BD Pyxis Mini Main REF: 349 Medication cabinet An FDA recall record reflects a firm removing or correcting a product already in distribution because it does not meet FDA requirements. On 2026-06-10, Argus HQ recorded a FDA recall for CareFusion 303, Inc., rated "high" severity in Argus HQ's classification: CareFusion 303, Inc. — Class II recall: BD Pyxis Anesthesia Station ES REF: 327 Medication cabinet An FDA recall record reflects a firm removing or correcting a product already in distribution because it does not meet FDA requirements. On 2026-06-10, Argus HQ recorded a FDA recall for CareFusion 303, Inc., rated "high" severity in Argus HQ's classification: CareFusion 303, Inc. — Class II recall: BD Pyxis MedBank Mini REF: 1147-00 Medication cabinet An FDA recall record reflects a firm removing or correcting a product already in distribution because it does not meet FDA requirements. On 2026-06-10, Argus HQ recorded a FDA recall for CareFusion 303, Inc., rated "high" severity in Argus HQ's classification: CareFusion 303, Inc. — Class II recall: BD Pyxis MedStation 4000 REF: 303 Medication cabinet An FDA recall record reflects a firm removing or correcting a product already in distribution because it does not meet FDA requirements. On 2026-06-10, Argus HQ recorded a FDA recall for CareFusion 303, Inc., rated "high" severity in Argus HQ's classification: CareFusion 303, Inc. — Class II recall: BD Pyxis MedStation ES Tower REF: 352 Medication cabinet An FDA recall record reflects a firm removing or correcting a product already in distribution because it does not meet FDA requirements. On 2026-06-10, Argus HQ recorded a FDA recall for CareFusion 303, Inc., rated "high" severity in Argus HQ's classification: CareFusion 303, Inc. — Class II recall: BD Pyxis Anesthesia Station 4000 REF: 338 Medication cabinet An FDA recall record reflects a firm removing or correcting a product already in distribution because it does not meet FDA requirements. On 2026-06-10, Argus HQ recorded a FDA recall for CareFusion 303, Inc., rated "high" severity in Argus HQ's classification: CareFusion 303, Inc. — Class II recall: BD Pyxis MedStation ES REF: 323 Medication cabinet An FDA recall record reflects a firm removing or correcting a product already in distribution because it does not meet FDA requirements. In total, CareFusion 303, Inc. has 8 FDA events on file with Argus HQ across the sources Argus HQ currently tracks (FDA Warning Letters, recalls, drug/biologic approvals, and Form 483 inspection observations).

Frequently asked questions

How many FDA actions does Argus HQ track for CareFusion 303, Inc.?

8 total: 0 warning letters, 8 recalls, 0 approval records, and 0 Form 483 inspection citations.

What is the most recent FDA action on file for CareFusion 303, Inc.?

June 10, 2026. Argus HQ ingests new FDA enforcement records daily.

Has CareFusion 303, Inc. had product recalls?

Yes, 8 recalls on file. See the full history below for each one.

Is this FDA enforcement data for CareFusion 303, Inc. official?

Every record links directly to its primary FDA.gov source. Argus HQ aggregates and structures public FDA data; the verbatim FDA record is always the source of truth.

Related enforcement actions

• CareFusion 303, Inc. — Class II recall: BD Pyxis MedStation ES REF: 323 Medication cabinet →
• CareFusion 303, Inc. — Class II recall: BD Pyxis Anesthesia Station 4000 REF: 338 Medication cabinet →
• CareFusion 303, Inc. — Class II recall: BD Pyxis MedStation ES Tower REF: 352 Medication cabinet →
• CareFusion 303, Inc. — Class II recall: BD Pyxis MedStation 4000 REF: 303 Medication cabinet →
• CareFusion 303, Inc. — Class II recall: BD Pyxis MedBank Mini REF: 1147-00 Medication cabinet →
• CareFusion 303, Inc. — Class II recall: BD Pyxis Anesthesia Station ES REF: 327 Medication cabinet →
• CareFusion 303, Inc. — Class II recall: BD Pyxis Mini Main REF: 349 Medication cabinet →
• CareFusion 303, Inc. — Class II recall: BD Pyxis MedBank Tower REF: 1145-00 Medication cabinet →

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