Skip to content
Back to recalls
Drug FDA Class III Ongoing Quality

Asmanex Twisthaler, mometasone furoate inhalation powder, 220 mcg per actuation, 14 Metered Doses, Rx Only, Manuf. for: Organon LLC, a subsidiary of Organon & Co. Product of Singapore. NDC 78206-114-03

Organon Llc Published Jun 19, 2024

Risk level

Class III

Unlikely to cause harm, but violates labeling or manufacturing rules.

Severity score 40/100

What should you do?

  • Check whether you have this product, using the lot codes, UPCs, and dates listed below.
  • Do not eat, serve, or sell the affected product.
  • Return it to the place of purchase for a refund, or throw it away in a sealed bag so people and animals can’t get to it.
  • Contact Organon Llc or your place of purchase with questions, and see the source record below for full details.
Reason for recall

Defective Container

Affected products (1)

Asmanex Twisthaler, mometasone furoate inhalation powder, 220 mcg per actuation, 14 Metered Doses, Rx Only, Manuf. for: Organon LLC, a subsidiary of Organon & Co. Product of Singapore. NDC 78206-114-03

ASMANEX · 2,551 units

NDC: 78206-114, 78206-115, 78206-114-03, 78206-114-04, 78206-114-02, 78206-114-01, 78206-114-59, 78206-115-59, 78206-115-01
Code info: Lot #: X024051, Exp 04/25/2025

Affected areas

Nationwide

Timeline

  1. Initiated
    May 28, 2024
  2. Published
    Jun 19, 2024
Recall number
D-0551-2024
Agency
U.S. Food and Drug Administration
Country
US
Source data (openFDA JSON) About FDA enforcement reports

FDA records come from the openFDA drug enforcement-report dataset — the agency's full weekly enforcement list. Most entries are not issued as consumer press releases, so they won't appear on fda.gov/recalls or in a web search. The source record link above resolves this exact recall by its number.