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

Is NDC 24357-0011-13 recalled?

Epinephrine Professional · 1 KIT in 1 CARTON (24357-011-13) * 1 mL in 1 VIAL (42023-159-25) * 1 mL in 1 PACKET (68599-5804-1)

Yes — this exact package was recalled

1 FDA recall names the code 24357-0011-13 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.

1 of these recalls is still ongoing.

Active ingredient
Epinephrine and Isopropyl Alcohol
Form
Kit · Intramuscular, Subcutaneous
Labeler
Focus Health Group
Type
Human Prescription Drug
Product code
24357-0011

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.