Class II · Moderate risk
Fentanyl Citrate Inj.
Lack of Assurance of Sterility; potential loose metal overseal crimp defects.
National Drug Code
Is NDC 0409-9094-12 recalled?
Fentanyl Citrate
Yes — this exact package was recalled
2 FDA recalls name the code 0409-9094-12 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
- Fentanyl Citrate
- Strength
- FENTANYL CITRATE 50 ug/mL
- Form
- Injection, Solution · Intramuscular, Intravenous
- Labeler
- Hospira, Inc.
- Type
- Human Prescription Drug · DEA CII
- Product code
- 0409-9094
Recalls naming this package
Class II · Moderate risk
Fentanyl Citrate Inj.
Defective Container: confirmed customer reports for vials with loose metal overseal crimp defects, which may result in lack of assurance of sterility.
Class II · Moderate risk
Fentanyl Citrate Injection
Lack of Assurance of Sterility; improperly crimped fliptop vials
Class II · Moderate risk
Fentanyl Citrate Injection
Lack of Assurance of Sterility: Fliptop vial crimps are loose or missing.
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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