FDA recall record

Zydus Pharmaceuticals (USA) Icosapent Ethyl capsules, 1 gram, 120-count bottles recall — FDA D-0295-2026

Subpotent Drug: Due to oxidation caused by leakage of the contents of the capsules

Class IIclassification
D-0295-2026official record ID
Jan 28, 2026report date

Recall record at a glance

Official recordD-0295-2026
CategoryDrug Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmZydus Pharmaceuticals (USA) Inc
Report dateJan 28, 2026
Recall initiation dateDec 30, 2025
Quantity22,896 bottles
LocationPennington, NJ, United States

Official product description

Icosapent Ethyl capsules, 1 gram, 120-count bottles, Rx only, Manufactured by: Softgel Healthcare Pvt. Ltd., India, Distributed by: Zydus Pharmaceuticals (USA) Inc., Pennington, NJ 08534, NDC 70710-1592-07

Why the product was recalled

Subpotent Drug: Due to oxidation caused by leakage of the contents of the capsules

Distribution information

US Nationwide.

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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