FlaggedRx← Medication recall checkHome
Class II · ModerateActive recall

Desmopressin Acetate

Could cause temporary or reversible harm; serious harm is unlikely.

Does this affect you?
Check your lot numberLot #: VM4231, Exp 06/30/2027
Where it was soldU.S.A. Nationwide
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.

What happened

Defective container: defect in a batch of bottle caps, specifically involving dislodged or missing cap liners.

What to do

  1. Check the lot number and expiry on your medicine against the recall above.
  2. Talk to your pharmacist or doctor before changing anything — don't stop on your own.
  3. Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).

Who makes it

Made byApotex Corp.
Brand nameDESMOPRESSIN ACETATE
Generic nameDESMOPRESSIN ACETATE
Active ingredient(s)DESMOPRESSIN ACETATE
Distributed by / forApotex Corp.
NDC60505-0815-0
Show the full FDA record
Full product labelDesmopressin 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
Recalling firmApotex Corp.
DistributionU.S.A. Nationwide
QuantityN/A
Recall initiated2026-04-08
Report date2026-04-22
Recall completed—
Recall numberD-0510-2026
ClassificationClass II
FDA statusOngoing
Origin on fileWeston FL United States

Related

Recent drug recallsCheck another medication

Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗

This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.