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

Is NDC 59579-0006 recalled?

Air

This product was recalled — in other package sizes

No FDA recall names your exact package code, but 1 recall cover the same product (59579-0006) in a different bottle or carton size. Worth checking with your pharmacist.

Active ingredient
Air
Strength
AIR 1000 mL/L
Form
Gas · Respiratory (inhalation)
Labeler
Linde Gas & Equipment Inc.
Type
Human Prescription Drug
Product code
59579-0006

Recalls of this product

Class III · Low risk

UN1002 Air

CGMP Deviations: Confirmed customer compliant of odor when turning on a cylinder of medical air.

Terminated cGMP deviation Praxair Inc. D-0782-2016

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.