How many FDA warning letters has International Medication Systems Ltd. received?

Argus HQ has not recorded an FDA warning letter for International Medication Systems Ltd. in our current dataset.

What FDA recalls has International Medication Systems Ltd. issued?

Argus HQ has recorded 1 FDA recall tied to International Medication Systems Ltd..

Is International Medication Systems Ltd. FDA compliant?

Argus HQ is not a compliance rating service. As of this page's last update, our dataset shows 0 warning letters, 1 recall, and 0 approval records for International Medication Systems Ltd.. Review the linked FDA source records directly before drawing a compliance conclusion.

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company

International Medication Systems Ltd.

Name: FDA Enforcement Actions Against International Medication Systems Ltd.
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 · drug_recall2026-04-22
International Medication Systems Ltd. — Class II recall: EPINEPHRINE Injection, USP, 1 mg/10mL (0.1 mg/mL), Rx only, INTERNATIONAL MEDICA…

Frequently asked questions

How many FDA warning letters has International Medication Systems Ltd. received?: Argus HQ has not recorded an FDA warning letter for International Medication Systems Ltd. in our current dataset.
What FDA recalls has International Medication Systems Ltd. issued?: Argus HQ has recorded 1 FDA recall tied to International Medication Systems Ltd..
Is International Medication Systems Ltd. FDA compliant?: Argus HQ is not a compliance rating service. As of this page's last update, our dataset shows 0 warning letters, 1 recall, and 0 approval records for International Medication Systems Ltd.. 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.