Class I ยท High risk
Optiray Imaging Bulk Package-350
Presence of Particulate Matter: comprising polyethylene and other plastic materials, stainless steel and glass.
National Drug Code
Is NDC 0019-1333-65 recalled?
Optiray 350 · 6 BOTTLE, GLASS in 1 CARTON (0019-1333-65) / 500 mL in 1 BOTTLE, GLASS
Yes — this exact package was recalled
1 FDA recall names the code 0019-1333-65 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.
1 of these recalls is still ongoing.
- Active ingredient
- Ioversol
- Strength
- IOVERSOL 741 mg/mL
- Form
- Injection · Intra-Arterial, Intravenous
- Labeler
- Liebel-Flarsheim Company LLC
- Type
- Human Prescription Drug
- Product code
- 0019-1333
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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