Zydus Pharmaceuticals (USA) Inc 2026-03-18 Health serious FDA
Health · FDA · Recall #FDA-D-0400-2026
Icosapent Ethyl Capsules, 1 gram, 120 Capsules per bottle, Rx only, Manufactured by:… Recall
Issued March 18, 2026 · Zydus Pharmaceuticals (USA) Inc
In March 2026, Zydus Pharmaceuticals (USA) Inc recalled the Icosapent Ethyl Capsules, 1 gram, 120 Capsules per bottle, Rx only, Manufactured by:…, a serious health recall reported by the FDA. Affected owners are eligible for a voluntary. Here is what the hazard is and exactly what to do about it.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Failed Tablet/Capsule specifications: Red dots inside capsule and melted capsule caused by oxidized Icosapent ethyl, the active ingredient.
What you should do
- 1 Stop using Icosapent Ethyl Capsules, 1 gram, 120 Capsules per bottle, Rx only, Manufactured by:… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Zydus Pharmaceuticals (USA) Inc to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Zydus Pharmaceuticals (USA) Inc
- Category
- Health
- Recall date
- March 18, 2026
- Units affected
- Not reported
- Sold at
- Nationwide in the USA
- Recall number
- FDA-D-0400-2026
- Made in
- United States
- Issuing agency
- FDA
In context
- Zydus Pharmaceuticals (USA) Inc has 31 recalls in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 356th Health recall we've logged in 2026.