CLASS II Drug recall · Reported 11 Dec 2024 · FDA Enforcement Report

Levothyroxine Sodium Tablets, USP, 75 mcg (0.075 mg) recalled

Accord Healthcare is recalling Levothyroxine Sodium Tablets, USP, 75 mcg (0.075 mg), distributed nationwide in the US. The recall was initiated on 8 Nov 2024 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot #: D2300191, Exp 12/31/2025
NDC16729-447, 16729-458, 16729-448, 16729-449, 16729-451, 16729-450
UPC0316729447157, 0316729449151, 0316729452151, 0316729454155, 0316729453158, 0316729448154

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

Recall details

Recall number
D-0076-2025
FDA event ID
95747
Recalling firm
Accord Healthcare, Raleigh, NC
Manufacturer
Accord Healthcare Inc.
Classification
Class II
Status
Terminated
Recall initiated
8 Nov 2024
FDA classified
29 Nov 2024
Reported
11 Dec 2024
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Potency & Assay

Timeline

8 Nov 2024Recall initiated by company
29 Nov 2024Classified by FDA+21 days
11 Dec 2024Published in enforcement report+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Subpotent drug

Potency and specification recalls happen when a batch tests outside its approved limits for strength, purity or dissolution, which can mean the dose delivered is higher or lower than labelled.

Product as listed by the FDA

Levothyroxine Sodium Tablets, USP, 75 mcg (0.075 mg), 1000-count bottle, Rx Only, Manufactured for: Accord Healthcare, Inc., Durham, NC 27703, Manufactured by: Intas Pharmaceuticals Limited, Camp Road, Selaqui, Dehradun-248 197, INDIA, NDC 16729-449-17

Where it was distributed

USA Nationwide

Nationwide

Questions about this recall

Why was it recalled?

Subpotent drug

Which lots are affected?

Lot #: D2300191, Exp 12/31/2025

Where was it sold?

USA Nationwide

What should I do if I have it?

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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