Class II · Moderate risk
0.9% Sodium Chloride Injection
Lack of Assurance of Sterility
National Drug Code
Is NDC 17271-0701-02 recalled?
Sodium chloride · 50 mL in 1 BAG (17271-701-02)
Yes — this exact package was recalled
1 FDA recall names the code 17271-0701-02 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.
4 of these recalls are still ongoing.
- Active ingredient
- Sodium Chloride
- Strength
- SODIUM CHLORIDE 9 mg/mL
- Form
- Injection, Solution · Intravenous
- Labeler
- Becton Dickinson and Company
- Type
- Human Prescription Drug
- Product code
- 17271-0701
Recalls naming this package
Class II · Moderate risk
0.9% Sodium Chloride Injection
Lack of Assurance of Sterility
Class II · Moderate risk
0.9% Sodium Chloride Injection
Lack of Assurance of Sterility
Class II · Moderate risk
0.9% Sodium Chloride Injection
Lack of Assurance of Sterility
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.
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