How many FDA warning letters has Magellan Diagnostics, Inc. received?

Argus HQ has not recorded an FDA warning letter for Magellan Diagnostics, Inc. in our current dataset.

What FDA recalls has Magellan Diagnostics, Inc. issued?

Argus HQ has recorded 3 FDA recalls tied to Magellan Diagnostics, Inc..

Is Magellan 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 Magellan Diagnostics, Inc.. Review the linked FDA source records directly before drawing a compliance conclusion.

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company

Magellan Diagnostics, Inc.

Name: FDA Enforcement Actions Against Magellan Diagnostics, Inc.
Creator: Argus HQ
License: https://argushq.ai/methodology

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_recall2026-04-29
Magellan Diagnostics, Inc. — Class II recall: LeadCare Ultra Blood Lead Test Kit; Catalog Number: 70-8098; The LeadCare Ultr…
fda_recall · device_recall2026-04-29
Magellan Diagnostics, Inc. — Class II recall: (1)(2) LeadCare¿ II Blood Lead Test Kit, (3)LeadCare¿ II 5X Blood Lead Test Kit,…
fda_recall · device_recall2026-04-29
Magellan Diagnostics, Inc. — Class II recall: LeadCare¿ Plus Blood Lead Test Kit; Catalog Number: 82-0004; The LeadCare¿ Plu…

Frequently asked questions

How many FDA warning letters has Magellan Diagnostics, Inc. received?: Argus HQ has not recorded an FDA warning letter for Magellan Diagnostics, Inc. in our current dataset.
What FDA recalls has Magellan Diagnostics, Inc. issued?: Argus HQ has recorded 3 FDA recalls tied to Magellan Diagnostics, Inc..
Is Magellan 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 Magellan 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.