The Harvard Drug Group LLC: 10 recalls on record

Recalls filed with 1 agency: FDA (10).

First recall on record: February 4, 2015. Most recent: July 1, 2026.

Risk classification: Class II: 9 · Class III: 1

Most recent recalls

DateAgencyProduct
July 1, 2026FDACarton Label: MAJOR, Methylergonovine Maleate Tablets, USP, 0.2 mg, 20 TABLETS (2 x 10), …D-0609-2026
April 29, 2026FDAOmega-3-Acid, Ethyl Esters, Capsules, USP, 1 gram, 50 capsules (5 x 10 unit dose blister …D-0493-2026
April 22, 2026FDAMemantine Hydrochloride Extended-Release, Capsules, 7 mg, 100 Capsules (10 x 10 blister p…D-0485-2026
March 11, 2026FDAMidodrine Hydrochloride Tablets, USP, 5 mg, 50 Tablets (5 x 10 blister packs), Rx only, P…D-0383-2026
October 29, 2025FDAGabapentin Capsules, USP, 100 mg, 100 Capsules (10 x 10 blister packs), Rx only, Packaged…D-0030-2026
October 29, 2025FDAGabapentin Capsules, USP, 100 mg, 10 Capsules (10 x 1 blister pack), Rx only, Packaged an…D-0031-2026
July 9, 2025FDAGabapentin Capsules, USP, 100 mg, 10 capsules (10x1) per bag, Rx only, Packaged and Distr…D-0508-2025
July 9, 2025FDAGabapentin Capsules, USP, 100 mg, 100 capsules (10x10), blister pack cartons, Rx only, Pa…D-0507-2025
July 8, 2015FDAOXYCODONE HCl C-II Tablets, 5 mg USP, 100-count blister cards, Rx only, Manufactured by N…D-1150-2015
February 4, 2015FDAThera Tablets with Beta Carotene Dietary SupplementF-0925-2015

Questions about this company

How many recalls does The Harvard Drug Group LLC have?
Recalert has 10 U.S. recalls on record for The Harvard Drug Group LLC, published between February 4, 2015 and July 1, 2026.
What was the most recent The Harvard Drug Group LLC recall?
FDA recall D-0609-2026, published July 1, 2026: Carton Label: MAJOR, Methylergonovine Maleate Tablets, USP, 0.2 mg, 20 TABLETS (2 x 10), Rx only, Packaged and Distributed by: MAJOR PHARMACEUTICALS, Indianapolis, in 46268, NDC 0904-7282-10. Bliste…
Which agencies have handled The Harvard Drug Group LLC recalls?
The Harvard Drug Group LLC appears as the recalling firm in recalls from: FDA (10).

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