Class II ยท Moderate risk
Omnipaque (iohexol)
Defective Container: vial defect was identified that could potentially impact the container closure and result in a lack of sterility assurance and/or the potential for glass particles.
National Drug Code
Is NDC 0407-1411-20 recalled?
Omnipaque
Yes — this exact package was recalled
1 FDA recall names the code 0407-1411-20 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.
- Active ingredient
- Iohexol
- Strength
- IOHEXOL 180 mg/mL
- Form
- Injection, Solution · Intrathecal, Oral, Rectal
- Labeler
- GE Healthcare Inc.
- Type
- Human Prescription Drug
- Product code
- 0407-1411
Recalls naming this package
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
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