Class I ยท High risk
Epinephrine Injection
Presence of Particulate Matter and Lack of Assurance of Sterility. Particulate matter identified as nylon, cellulosic, acrylic, polyethylene and glass and broken and leaking vials.
National Drug Code
Is NDC 0517-3030-01 recalled?
Epinephrine · 1 VIAL in 1 CARTON (0517-3030-01) / 1 mL in 1 VIAL
Yes — this exact package was recalled
1 FDA recall names the code 0517-3030-01 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
- epinephrine
- Strength
- EPINEPHRINE 1 mg/mL
- Form
- Injection · Intramuscular, Intravenous, Subcutaneous
- Labeler
- American Regent, Inc.
- Type
- Human Prescription Drug
- Product code
- 0517-3030
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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