RecallRadar

FDA Drug recall D-0510-2026

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…

On 2026-04-22 the FDA classified a Class II recall of 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… by Apotex, citing defective container: defect in a batch of bottle caps, specifically involving dislodged or missing cap liners.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0510-2026
ClassificationClass II
Statusongoing
Initiated2026-04-08
Published2026-04-22
Last updated2026-09-13 11:52 UTC
CompanyApotex
DistributionUS

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.

Identifiers

ndc60505-0815-0
code_infoLot #: VM4231, Exp 06/30/2027

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0510-2026%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.