Apotex Corp.: Desmopressin Nasal Spray, Usp, 10 Mcg/0

Desmopressin Nasal Spray Recall Summary Apotex Corp. is recalling Desmopressin Nasal Spray (10 mcg/0.1 mL, 5 mL bottles) nationwide because some bottle caps have defective liners that may be dislodged or missing. This is a Class II recall, meaning the product could cause temporary or medically reversible adverse effects. The affected medication was distributed across all U.S. states and the District of Columbia.

Recalling firm
Apotex Corp.
Product
Desmopressin Nasal Spray, USP, 10 mcg/0.1 mL, 5 mL bottle (50 doses), Rx only, Mfg by: Apotek inc., Toronto, Ontario, Canada, M9L 1T9, Mfg for: Apotek Corp., Weston, FL 33326, NDC 60505-0815-0
Reason
Defective container: defect in a batch of bottle caps, specifically involving dislodged or missing cap liners.
Classification
Class II
Category
drug recall
Country
United States
Agency
U.S. Food and Drug Administration
Recall date
2026-04-08
Status
Ongoing
Areas affected
AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
Distribution
U.S.A. Nationwide

Official recall notice from U.S. Food and Drug Administration

Recall details on Nibble Recalls: https://trynibble.app/recalls/7824fd2f-45d2-4a97-b69c-eef1ce35940a