Omnipaque (iohexol) Injection, 180mgI/mL, 20 mL Single-Dose Vial, packaged in 10 x 20 mL Vials per carton, Rx only, Distributed by GE Healthcare Inc., Marlborough, MA 01752 U.S.A.; Manufactured by GE Healthcare AS, Oslo, Norway; NDC 0407-1411-20.
Drug Recall
Official source record
- Recall number
- D-0319-2019
- Event ID
- 81691
- Classification
- Class II
- Status
- Terminated
- Recalling company
- GE Healthcare Inc. Life Sciences
- Reason for recall
- 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.
- Report date
- December 26, 2018
- Recall initiation date
- October 29, 2018
- Termination date
- October 30, 2023
- Distribution pattern
- TN
Drug product identifiers
- Manufacturer
- GE Healthcare Inc.
- Brand name
- OMNIPAQUE
- Generic name
- IOHEXOL
- Substance name
- IOHEXOL
- Product NDCs
- 0407-1401; 0407-1411; 0407-1412; 0407-1413; 0407-1414; 0407-1415; 0407-1416
- Package NDCs
- 0407-1401-52; 0407-1411-10; 0407-1411-20; 0407-1412-10; 0407-1412-20; 0407-1412-27; 0407-1412-28; 0407-1412-29; 0407-1412-30; 0407-1412-33; 0407-1412-34; 0407-1412-35; 0407-1412-49; 0407-1412-50; 0407-1412-60; 0407-1413-10; 0407-1413-11; 0407-1413-30; 0407-1413-50; 0407-1413-51; 0407-1413-53; 0407-1413-59; 0407-1413-60; 0407-1413-61; 0407-1413-62; 0407-1413-63; 0407-1413-65; 0407-1413-66; 0407-1413-69; 0407-1413-90; 0407-1413-91; 0407-1413-92; 0407-1413-93; 0407-1413-95; 0407-1413-96; 0407-1413-98; 0407-1413-99; 0407-1414-03; 0407-1414-04; 0407-1414-20; 0407-1414-21; 0407-1414-22; 0407-1414-23; 0407-1414-24; 0407-1414-50; 0407-1414-51; 0407-1414-52; 0407-1414-53; 0407-1414-60; 0407-1414-76; 0407-1414-80; 0407-1414-89; 0407-1414-90; 0407-1414-91; 0407-1414-93; 0407-1414-94; 0407-1414-95; 0407-1415-09; 0407-1416-12
- Routes
- INTRAVASCULAR; INTRAVENOUS
Where this information comes from
View FDA enforcement record -- the specific openFDA drug enforcement record this summary was built from.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Drug recall information is sourced from the FDA's structured openFDA Enforcement Reports. Newly announced recalls may appear on FDA.gov before they become available in the structured dataset. See Methodology for details.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class II mean?
A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.
Is this recall still active?
According to the FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this medication?
Do not start, stop, or change any medication based on this page. Follow the instructions published by the FDA and the recalling company (see the source links below), and talk to your pharmacist or physician if you have questions about a specific medication.
Where can I find more official information?
The source links below, published by the FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
Public Health Trace republishes official FDA drug recall information -- it is not affiliated with the FDA, does not verify or supplement what the source has published, and does not provide medical advice. Never start, stop, or change a medication based on this page. Always follow the guidance of your pharmacist or physician, and consult the official source links above for the most current information. Read the full medical disclaimer.
