FDA Drug Recalls

Recalls / Class II

Class IID-0397-2025

Product

Levothyroxine Sodium Tablets, USP, 112 mcg (0.112 mg), 90 bottles, Rx Only, Manufactured for Accord Healthcare, Inc., Raleigh, NC 27617, Manufactured by: Intas Pharmaceuticals Limited, Camp Road, Selaqui, Dehradun-248 197, INDIA, NDC 16729-452-15

Brand name
Levothyroxine Sodium
Generic name
Levothyroxine Sodium
Active ingredient
Levothyroxine Sodium
Route
Oral
NDCs
16729-447, 16729-458, 16729-448, 16729-449, 16729-451, 16729-450, 16729-452, 16729-453, 16729-454, 16729-455 +2 more
FDA application
ANDA212399
Affected lot / code info
Lot # D2400725, Exp Date: 03/2026

Why it was recalled

Subpotent

Recalling firm

Firm
ACCORD HEALTHCARE, INC.
Manufacturer
Accord Healthcare Inc.
Notification channel
Letter
Type
Voluntary: Firm initiated
Address
8041 Arco Corporate Dr Ste 200, N/A, Raleigh, North Carolina 27617-2010

Distribution

Quantity
18,984 Bottles
Distribution pattern
Nationwide US.

Timeline

Recall initiated
2025-04-10
FDA classified
2025-04-30
Posted by FDA
2025-05-07
Status
Ongoing

Source: openFDA Drug Enforcement endpoint. Recall record D-0397-2025. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.

Class II recall: Levothyroxine Sodium · FDA Drug Recalls