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

Is NDC 0338-0117-03 recalled?

Lactated Ringers · 500 mL in 1 BAG (0338-0117-03)

Yes — this exact package was recalled

1 FDA recall names the code 0338-0117-03 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
Sodium chloride, potassium chloride, sodium lactate and calcium chloride
Strength
SODIUM CHLORIDE 600 mg/100mL; SODIUM LACTATE 310 mg/100mL…
Form
Injection, Solution · Intravenous
Labeler
Baxter Healthcare Company
Type
Human Prescription Drug
Product code
0338-0117

Recalls naming this package

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