Class II · Moderate risk
DOBUTamine Injection
Discoloration; discolored solution from cracked vials
National Drug Code
Is NDC 0409-2344-62 recalled?
Dobutamine
Yes — this exact package was recalled
1 FDA recall names the code 0409-2344-62 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
- Dobutamine
- Strength
- DOBUTAMINE HYDROCHLORIDE 12.5 mg/mL
- Form
- Injection, Solution, Concentrate · Intravenous
- Labeler
- Hospira, Inc.
- Type
- Human Prescription Drug
- Product code
- 0409-2344
Recalls naming this package
Class I · High risk
DOBUTamine Injection
Presence of Particulate Matter: Discolored solution due to a chip in the glass at the neck of the vial, also glass particulate was found within the solution.
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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