company
Siemens Healthcare Diagnostics, 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_recall2026-06-17Siemens Healthcare Diagnostics, Inc. — Class II recall: Siemens Dimension Tacrolimus Flex Reagent Cartridge (TAC), REF DF207, SMN 107007…
- fda_recall · device_recall2026-05-06Siemens Healthcare Diagnostics Inc — Class II recall: epoc BGEM BUN Test Card (25 pk) for the epoc Blood Analysis System; Siemens Ma…
- fda_recall · device_recall2026-05-06Siemens Healthcare Diagnostics, Inc. — Class II recall: Dimension Creatinine Flex reagent cartridge. Material Number: 10872079.
Frequently asked questions
- How many FDA warning letters has Siemens Healthcare Diagnostics, Inc. received?
- Argus HQ has not recorded an FDA warning letter for Siemens Healthcare Diagnostics, Inc. in our current dataset.
- What FDA recalls has Siemens Healthcare Diagnostics, Inc. issued?
- Argus HQ has recorded 3 FDA recalls tied to Siemens Healthcare Diagnostics, Inc..
- Is Siemens Healthcare Diagnostics, 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 Siemens Healthcare Diagnostics, 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.

