FDA recall record

Mirabegron Extended-Release Tablets, 25 mg, 30-count bottle recall — FDA D-0745-2026

CGMP: Due to Out of Specification (OOS) result for N-Nitroso Mirabegron impurity.

Class IIclassification
D-0745-2026official record ID
Aug 12, 2026report date

Recall record at a glance

Official recordD-0745-2026
CategoryDrug Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmZydus Pharmaceuticals (USA) Inc
Report dateAug 12, 2026
Recall initiation dateAug 5, 2026
LocationPennington, NJ, United States

Official product description

Mirabegron Extended-Release Tablets, 25 mg, 30-count bottle, Rx only, Manufactured by: Zydus Lifesciences Ltd., Matoda, Ahmedabad, India, Distributed by: Zydus Pharmaceuticals (USA) Inc., Pennington, NJ 08534, NDC 70710-1159-3.

Why the product was recalled

CGMP: Due to Out of Specification (OOS) result for N-Nitroso Mirabegron impurity.

Distribution information

Nationwide in the USA

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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