Fresh Recalls

FDAClass II · Drug · Recall D-0656-2026 · Recalled July 8, 2026

Levothyroxine Sodium Tablets recall — ACCORD HEALTHCARE, INC.

Agency report date: July 8, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named
Levothyroxine Sodium Tablets
Company / brand
ACCORD HEALTHCARE
Lot / serial / date codes
Lot # D2401522, Exp Date: 06/2026.
Distribution
US Nationwide.
Agency product description and boundaries

Levothyroxine Sodium Tablets, USP, 300 mcg (0.3mg), 90 Tablets bottles, Rx only, Manufactured for: Accord Healthcare, Inc., Raleigh, NC 27617, Manufactured by: lntas Pharmaceuticals Limited, Camp Road, Selaqui, Dehradun-248 197, INDIA, NDC 16729-458-15.

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

FDA reports: Subpotent Drug

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class II: may cause temporary or medically reversible health consequences.

Affected product: Levothyroxine Sodium Tablets

3. Open the official notice or contact

Official recall ID
D-0656-2026
Brand
ACCORD HEALTHCARE
Classification
Class II
Units affected
6432 bottles
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
Raleigh, NC, United States
Firm address
8041 Arco Corporate Dr Ste 200, N/A, 27617-2010

Identifying details (verbatim from the notice)

Product codes / lots
Lot # D2401522, Exp Date: 06/2026.
Distribution
US Nationwide.
Firm notified the public via
Letter
FDA event ID
99194
Recall initiated
June 8, 2026
FDA classified
June 30, 2026
FDA report date
July 8, 2026
Verify with the official sources:

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Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked September 7, 2026 at 6:00 AM UTC. Record retrieved September 7, 2026 at 6:00 AM UTC.

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