Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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National Drug Code

Is NDC 49230-0300-10 recalled?

Sodium Chloride · 12 BAG in 1 CARTON (49230-300-10) / 1000 mL in 1 BAG

Yes — this exact package was recalled

5 FDA recalls name the code 49230-0300-10 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.

3 of these recalls are still ongoing.

Active ingredient
Sodium Chloride
Strength
SODIUM CHLORIDE 900 mg/100mL
Form
Injection · Intravenous
Labeler
Fresenius Medical Care Renal Therapies Group, LLC
Type
Human Prescription Drug
Product code
49230-0300

Recalls naming this package

Class II · Moderate risk

Sodium Chloride 0.9% Injection

Lack of assurance of sterility: The product was potentially exposed to below-recommended storage temperatures, which may cause leaks in the packaging.

Terminated Sterility / contamination Fresenius Medical Care Holdings, Inc. NDC 49230-300-10 D-0777-2023
Class II · Moderate risk

0.9% Sodium Chloride Injection

Lack of Assurance of Sterility: Leakage of 0.9% Sodium Chloride for Injection, 1L, 12pk Saline Solution.

Ongoing Sterility / contamination Fresenius Medical Care Holdings, Inc. NDC 49230-300-10 D-0075-2023
Class II · Moderate risk

0.9% Sodium Chloride Injection

Lack of Assurance of Sterility: Leakage of 0.9% Sodium Chloride for Injection, 1L, 12pk Saline Solution.

Ongoing Sterility / contamination Fresenius Medical Care Holdings, Inc. NDC 49230-300-10 D-0015-2023

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