D-0552-2024 Class III Ongoing

Recalled by Organon Llc — Jersey City, NJ

FDA drug recall D-0552-2024 was initiated by Organon Llc on May 28, 2024 and is designated Class III. Reason for recall: Defective Container The recall status is ongoing. Affected quantity: 0.

Recall Details

Product Type
Drugs
Report Date
June 19, 2024
Initiation Date
May 28, 2024
Termination Date
N/A
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
0

Product Description

Asmanex Twisthaler, mometasone furoate inhalation powder, 220 mcg per actuation, 30 Metered Doses, Rx Only, Manuf. for: Organon LLC, a subsidiary of Organon & Co. Product of Singapore. NDC 78206-0114-04

Reason for Recall

Defective Container

Distribution Pattern

Nationwide in the USA

Code Information

Lot #: Y000085, Exp 4/25/2025