Class II ยท Moderate risk
Optiray 320
Labeling: Not Elsewhere Classified: RFID formatting error which reads product in Ultraject syringe as expired and will not allow injection of product by the Optivantage injector.
National Drug Code
Is NDC 0019-1323-00 recalled?
Optiray 320 · 20 SYRINGE, PLASTIC in 1 CARTON (0019-1323-00) / 100 mL in 1 SYRINGE, PLASTIC
Yes — this exact package was recalled
1 FDA recall names the code 0019-1323-00 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
- Ioversol
- Strength
- IOVERSOL 678 mg/mL
- Form
- Injection · Intra-Arterial, Intravenous
- Labeler
- Liebel-Flarsheim Company LLC
- Type
- Human Prescription Drug
- Product code
- 0019-1323
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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