Class III โ€” Low Risk

Low risk โ€” use of or exposure to this product is not likely to cause adverse health consequences.

UN1002 Air Recalled by Praxair Inc. Due to CGMP Deviations: Confirmed customer compliant of odor when...

Date: September 16, 2015
Company: Praxair Inc.
Status: Terminated
Source: FDA (Drug)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Praxair Inc. directly.

Affected Products

UN1002 Air, Compressed, Breathing Grade, USP, Distributed by Praxair Distribution, Inc. Roseville, MN 55113, NDC 59579-006.

Quantity: 127 cylinders

Why Was This Recalled?

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

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Praxair Inc.

Praxair Inc. has 3 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report