Class II · Moderate risk
Furosemide Injection
Lack of Assurance of Sterility: Loose crimp applied to the fliptop vial.
National Drug Code
Is NDC 0409-6102-04 recalled?
Furosemide · 25 VIAL, SINGLE-DOSE in 1 TRAY (0409-6102-04) / 4 mL in 1 VIAL, SINGLE-DOSE (0409-6102-18)
Yes — this exact package was recalled
2 FDA recalls name the code 0409-6102-04 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
- furosemide
- Strength
- FUROSEMIDE 10 mg/mL
- Form
- Injection, Solution · Intramuscular, Intravenous
- Labeler
- Hospira, Inc.
- Type
- Human Prescription Drug
- Product code
- 0409-6102
Recalls naming this package
Class II · Moderate risk
Furosemide Injection USP
Lack of Assurance of Sterility; possible loose crimp applied to fliptop vial
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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