Class II · Moderate risk
Icosapent Ethyl Capsules
Failed Tablet/Capsule specifications: Red dots inside capsule and melted capsule caused by oxidized Icosapent ethyl, the active ingredient.
National Drug Code
Is NDC 70710-1592-07 recalled?
icosapent ethyl · 120 CAPSULE in 1 BOTTLE (70710-1592-7)
Yes — this exact package was recalled
3 FDA recalls name the code 70710-1592-07 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.
2 of these recalls are still ongoing.
- Active ingredient
- icosapent ethyl
- Strength
- ICOSAPENT ETHYL 1 g/1
- Form
- Capsule · Oral
- Labeler
- Zydus Pharmaceuticals USA Inc.
- Type
- Human Prescription Drug
- Product code
- 70710-1592
Recalls naming this package
Class II · Moderate risk
Icosapent Ethyl capsules
Subpotent Drug: Due to oxidation caused by leakage of the contents of the capsules
Class II · Moderate risk
Icosapent Ethyl Capsules 1 gram
Failed Tablet/Capsule specifications; a product complaint was reported for burnt or melted capsules. This was determined to be a result of oxidation by leakage of capsule contents.
Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.
Other recalled products from this labeler
- 70710-1129 Chlorpromazine hydrochloride 2
- 70710-1047 Erythromycin 1
- 70710-1048 Erythromycin 1
- 70710-1130 Chlorpromazine hydrochloride 1
- 70710-1131 Chlorpromazine hydrochloride 1
- 70710-1132 Chlorpromazine hydrochloride 1
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