Class I · High risk
0.9% Sodium Chloride Injection USP
Presence of Particulate Matter.
National Drug Code
Is NDC 0264-7800-00 recalled?
Sodium Chloride · 12 CONTAINER in 1 CASE (0264-7800-00) / 1000 mL in 1 CONTAINER
Yes — this exact package was recalled
1 FDA recall names the code 0264-7800-00 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 g/100mL
- Form
- Injection, Solution · Intravenous
- Labeler
- B. Braun Medical Inc.
- Type
- Human Prescription Drug
- Product code
- 0264-7800
Recalls naming this package
Class II · Moderate risk
0.9% Sodium Chloride Injection USP
Lack of Assurance of Sterility; potential for fluid leakage at one of the weld sites.
Class II · Moderate risk
0.9% Sodium Chloride Injection USP
Lack of assurance of sterility: pinholes, within the finger boxes used during Form Fill Seal process resulting in leaks.
Class I · High risk
0.9% Sodium Chloride Injection USP
Presence of Particulate Matter
Class II · Moderate risk
0.9% Sodium Chloride Injection USP
Lack of sterility assurance: leaking bags
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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