Organon Llc: Drug Recall
Recall #D-0550-2024 · 05/28/2024
Class III: Low Risk
Recall Details
- Recall Number
- D-0550-2024
- Classification
- Class III
- Product Type
- Drug
- Recalling Firm
- Organon Llc
- Status
- Ongoing
- Date Initiated
- 05/28/2024
- Location
- Jersey City, NJ, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 2,886 units
Reason for Recall
Defective Container
Product Description
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
Distribution Pattern
Nationwide in the USA
Other Recalls by Organon Llc
- Class III: Low Risk 05/28/2024
- Class III: Low Risk 05/28/2024
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.