Class II · Moderate risk
Diazepam Injection
Lack of assurance of sterility: ineffective crimp on fliptop vials that may result in leaking at the neck of the vials.
National Drug Code
Is NDC 0409-3213-12 recalled?
Diazepam · 10 VIAL, MULTI-DOSE in 1 BOX (0409-3213-12) / 10 mL in 1 VIAL, MULTI-DOSE (0409-3213-11)
Yes — this exact package was recalled
4 FDA recalls name the code 0409-3213-12 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
- Diazepam
- Strength
- DIAZEPAM 5 mg/mL
- Form
- Injection, Solution · Intramuscular, Intravenous
- Labeler
- Hospira, Inc.
- Type
- Human Prescription Drug · DEA CIV
- Product code
- 0409-3213
Recalls naming this package
Class II · Moderate risk
Diazepam Injection
Lack of Assurance of Sterility: Loose crimp applied to the fliptop vial.
Class II · Moderate risk
Diazepam Injection
Lack of Assurance of Sterility: Loose crimp applied to the fliptop vial.
Class II · Moderate risk
Diazepam Injection
Lack of Assurance of Sterility: Loose crimp applied to the 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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