Class III โ€” Low Risk

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

Asmanex Twisthaler Recalled by Organon Llc Due to Defective Container

Date: May 28, 2024
Company: Organon Llc
Status: Ongoing
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 Organon Llc directly.

Affected Products

Asmanex Twisthaler, mometasone furoate inhalation powder, 220 mcg per actuation, 60 Metered Doses, Rx Only, Manuf. for: Organon LLC, a subsidiary of Organon & Co. Product of Singapore. NDC 78206-114-02

Quantity: 2,886 units

Why Was This Recalled?

Defective Container

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Organon Llc

Organon Llc has 3 total recalls tracked by RecallDetector.

Related Recalls

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