RecallRadar

FDA Drug recall D-0702-2026

Levothyroxine Sodium Tablets, USP, 75 mcg (0.075 mg), 100 Tablets (10 x 10 unit dose blisters) per carton, Rx only, Packaged and Distribute…

On 2026-07-29 the FDA classified a Class II recall of Levothyroxine Sodium Tablets, USP, 75 mcg (0.075 mg), 100 Tablets (10 x 10 unit dose blisters) per carton, Rx only, Packaged and Distribute… by Major Pharmaceuticals, citing subpotent Drug.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0702-2026
ClassificationClass II
Statusongoing
Initiated2026-07-13
Published2026-07-29
Last updated2026-09-13 11:52 UTC
CompanyMajor Pharmaceuticals
DistributionUS

Product

Levothyroxine Sodium Tablets, USP, 75 mcg (0.075 mg), 100 Tablets (10 x 10 unit dose blisters) per carton, Rx only, Packaged and Distributed by: MAJOR PHARMACEUTICALS, Indianapolis, IN 46268 USA. NDC: 0904-6951-61

Reason

Subpotent Drug

Identifiers

ndc0904-6949-61
ndc0904-6950-61
ndc0904-6951-61
ndc0904-6952-61
ndc0904-6953-61
ndc0904-6954-61
ndc0904-6955-61
ndc0904-6956-61
ndc0904-6957-61
code_infoLot# N02172, exp 07/2026; N02296, N02288, Exp. Date 12/2026

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0702-2026%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.