company
Beckman Coulter, 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_recall2026-04-29Beckman Coulter, Inc. — Class II recall: Access Total T4 Calibrator, Catalog No. 33805
- fda_recall · device_recall2026-04-15Beckman Coulter, Inc. — Class II recall: MicroScan Neg Multidrug Resistant MIC 1 REF C32368 UDI-DI code: 15099590720568…
- fda_recall · device_recall2026-04-15Beckman Coulter, Inc. — Class II recall: MicroScan Neg MIC 3J REF C54814
Frequently asked questions
- How many FDA warning letters has Beckman Coulter, Inc. received?
- Argus HQ has not recorded an FDA warning letter for Beckman Coulter, Inc. in our current dataset.
- What FDA recalls has Beckman Coulter, Inc. issued?
- Argus HQ has recorded 3 FDA recalls tied to Beckman Coulter, Inc..
- Is Beckman Coulter, Inc. FDA compliant?
- Argus HQ is not a compliance rating service. As of this page's last update, our dataset shows 0 warning letters, 3 recalls, and 0 approval records for Beckman Coulter, 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.