How many FDA warning letters has Medical Action Industries, Inc. 306 received?

Argus HQ has not recorded an FDA warning letter for Medical Action Industries, Inc. 306 in our current dataset.

What FDA recalls has Medical Action Industries, Inc. 306 issued?

Argus HQ has recorded 1 FDA recall tied to Medical Action Industries, Inc. 306.

Is Medical Action Industries, Inc. 306 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 Medical Action Industries, Inc. 306. Review the linked FDA source records directly before drawing a compliance conclusion.

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company

Medical Action Industries, Inc. 306

Name: FDA Enforcement Actions Against Medical Action Industries, Inc. 306
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_recall2026-05-13
Medical Action Industries, Inc. 306 — Class I recall: Medical Action Industries Inc. Pack Cath BHH, REF: BHCA49K, Sterile EO, Rx O…

Frequently asked questions

How many FDA warning letters has Medical Action Industries, Inc. 306 received?: Argus HQ has not recorded an FDA warning letter for Medical Action Industries, Inc. 306 in our current dataset.
What FDA recalls has Medical Action Industries, Inc. 306 issued?: Argus HQ has recorded 1 FDA recall tied to Medical Action Industries, Inc. 306.
Is Medical Action Industries, Inc. 306 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 Medical Action Industries, Inc. 306. 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.