Class II · Moderate risk
Ondansetron Injection
Presence of Particular Matter: Potential vendor glass issue - glass spiticules (glass strands) were identified during site inspection of the vials.
National Drug Code
Is NDC 0409-4755-03 recalled?
Ondansetron · 25 VIAL, SINGLE-DOSE in 1 TRAY (0409-4755-03) / 2 mL in 1 VIAL, SINGLE-DOSE (0409-4755-18)
Yes — this exact package was recalled
2 FDA recalls name the code 0409-4755-03 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
- Ondansetron
- Strength
- ONDANSETRON HYDROCHLORIDE 2 mg/mL
- Form
- Injection, Solution · Intramuscular, Intravenous
- Labeler
- Hospira, Inc.
- Type
- Human Prescription Drug
- Product code
- 0409-4755
Recalls naming this package
Class II · Moderate risk
Ondansetron Injection
Presence of Particulate; lot being recalled as a precaution due to the discovery of 2 particles found in a lot which preceded the recalled lot
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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