How many FDA warning letters has The Harvard Drug Group LLC received?

Argus HQ has not recorded an FDA warning letter for The Harvard Drug Group LLC in our current dataset.

What FDA recalls has The Harvard Drug Group LLC issued?

Argus HQ has recorded 3 FDA recalls tied to The Harvard Drug Group LLC.

Is The Harvard Drug Group LLC 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 The Harvard Drug Group LLC. Review the linked FDA source records directly before drawing a compliance conclusion.

.hq

company

The Harvard Drug Group LLC

Name: FDA Enforcement Actions Against The Harvard Drug Group LLC
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_recall2026-07-01
The Harvard Drug Group LLC — Class II recall: Carton Label: MAJOR, Methylergonovine Maleate Tablets, USP, 0.2 mg, 20 TABLETS (…
fda_recall · drug_recall2026-04-29
The Harvard Drug Group LLC — Class II recall: Omega-3-Acid, Ethyl Esters, Capsules, USP, 1 gram, 50 capsules (5 x 10 unit dose…
fda_recall · drug_recall2026-04-22
The Harvard Drug Group LLC — Class II recall: Memantine Hydrochloride Extended-Release, Capsules, 7 mg, 100 Capsules (10 x 10…

Frequently asked questions

How many FDA warning letters has The Harvard Drug Group LLC received?: Argus HQ has not recorded an FDA warning letter for The Harvard Drug Group LLC in our current dataset.
What FDA recalls has The Harvard Drug Group LLC issued?: Argus HQ has recorded 3 FDA recalls tied to The Harvard Drug Group LLC.
Is The Harvard Drug Group LLC 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 The Harvard Drug Group LLC. 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.