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Medium risk Drugs & MedicationsClass II

Apotex Desmopressin Nasal Spray Recall

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 f

Updated April 8, 2026

Apotex is recalling Desmopressin Nasal Spray due to defective bottle caps with dislodged or missing cap liners, which could compromise the integrity of the medication and affect proper dosing.

Is the Apotex Corp. recalled? Yes. This product was recalled by FDA on April 8, 2026. Details below.

What is recalled

Desmopressin Nasal Spray, USP, 10 mcg/0.1 mL, 5 mL bottles (50 doses), NDC 60505-0815-0, manufactured by Apotex Inc., Toronto, Ontario, Canada for Apotex Corp., Weston, FL 33326.

Am I affected

You're affected if you have a prescription bottle of Desmopressin Nasal Spray with NDC 60505-0815-0. Check the label on your bottle, specifically look for any loose, missing, or damaged cap liners.

What to do right now

Contact your pharmacy or doctor immediately. Do not use the product if the cap liner is dislodged or missing. Your healthcare provider or pharmacist can confirm whether your bottle is affected and provide a replacement if needed.

The hazard

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

Brands affected

Apotex Corp.
Source
FDA
Category
Drugs & Medications
Recall ID
fda-D-0510-2026
Classification
Class II
Recalled
April 8, 2026
Read the official notice

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