Class II · Moderate risk
5% Dextrose Injection
Lack of sterility assurance: bag has the potential to leak.
National Drug Code
Is NDC 0409-7100-68 recalled?
Dextrose
Yes — this exact package was recalled
1 FDA recall names the code 0409-7100-68 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
- dextrose monohydrate
- Strength
- DEXTROSE MONOHYDRATE 50 mg/mL
- Form
- Injection, Solution · Intravenous
- Labeler
- Hospira, Inc.
- Type
- Human Prescription Drug
- Product code
- 0409-7100
Recalls naming this package
Class II · Moderate risk
5% DEXTROSE Injection
Lack of Assurance of Sterility: there is a potential for solution to leak at the administrative port of the primary container.
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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