Apotex Corp. Desmopressin Nasal Spray, USP, 10 mcg/0.1 mL, 5 mL bottle recall: Defective container: defect in a batch of bottle caps
Defective container: defect in a batch of bottle caps, specifically involving dislodged or missing cap liners.
The hazard: Drug safety concern
The product was withdrawn from distribution. Whether your own pack is affected comes down to the lot number.
What the notice says: Defective container: defect in a batch of bottle caps, specifically involving dislodged or missing cap liners.
Why it matters: The FDA recorded an enforcement action against this product. The classification and the summary above describe how serious the agency considers it.
Recall details
- Recall number
- D-0510-2026
- Published
- April 22, 2026
- Risk level
- Class II
- Status
- Ongoing
- Issued by
- U.S. Food and Drug Administration
- Brand
- Apotex Corp.
- Product type
- Prescription & OTC drugs
- Units affected
- N/A
- Distribution
- Nationwide
- Made in
- United States
- Lot / code info
- Lot #: VM4231, Exp 06/30/2027
Products covered by this 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 for: Apotek Corp., Weston, FL 33326, NDC 60505-0815-0
Check your product
The notice names 11 codes you can read straight off the package. Type the one printed on yours and the list below narrows to it.
Lot or batch code
Usually ink-stamped near the seam, the cap or the bottom of the pack.
- VM4231
- Exp 06
- 30
- 2027 — N
Best-by / use-by date
Printed beside the lot code, not on the price sticker.
- 06
- 30
- 2027 — N
NDC number
On the carton and again on the bottle or blister label.
- 60505-0815-0
Package size
Match the net weight or the piece count on the front of the pack.
- 0.1 mL
- 5 mL
- 9 L
Codes are lifted verbatim from the FDA — Drug enforcement notice. A code that is missing here may still be covered — the official notice is the complete list.
What to do about Drug safety
Apotex Corp. — The product was withdrawn from distribution. Whether your own pack is affected comes down to the lot number.
- Check the lot number on your pack against the codes listed above.
- Keep the carton; the lot number is often printed only on the outer pack.
- Report side effects you think the product caused to FDA MedWatch.
- Do not stop a prescribed medicine on your own — speak to your prescriber or pharmacist first.
What the company owes you
A recalled medicine is the manufacturer’s cost to carry, not yours or your pharmacist’s.
- The purchase price or co-pay is refundable, and so is the cost of returning the product if they ask you to ship it.
- Ask the pharmacy to handle the claim where they can — they process recall returns in bulk and it saves you the correspondence.
- Keep the carton, the leaflet and the pharmacy label together until the claim is closed.
- Costs beyond the price of the medicine need to go to the company directly, in writing, with the recall number quoted.
Company contact: Apotex Corp. — 2400 N Commerce Pkwy Ste 400, Weston, FL, 33326-3253
The official notice
This page summarises a notice published by U.S. Food and Drug Administration. The agency notice is the authoritative version — read it before you act, and treat it as the final word if anything here looks different.
Open the FDA — Drug enforcement record U.S. Food and Drug Administration recalls
Questions people ask about this recall
Why was Apotex Corp. prescription & otc drugs recalled?
Defective container: defect in a batch of bottle caps, specifically involving dislodged or missing cap liners. Defective container: defect in a batch of bottle caps, specifically involving dislodged or missing cap liners.
How do I know if I have the recalled product?
Match the codes printed on your package against the notice: lot code VM4231, Exp 06, 30; best-by date 06 or 30. If the code on your package is not on that list, your unit is outside the recall.
What should I do with it right now?
Check the lot number on your pack against the codes listed above.
Can I get my money back?
The purchase price or co-pay is refundable, and so is the cost of returning the product if they ask you to ship it.
Where was the recalled product sold?
It was distributed nationwide.
Related recalls
-
Class II · 18 days ago
Apotex Corp. Paroxetine Extended-Release Tablets, 37.5mg, 30-count bottle recall: Failed dissolution specifications
Failed dissolution specifications.
-
Class II · last month
Apotex Corp. Paxil CR, Paroxetine, Extended-Release Tablets, 37.5mg, 30 count bottle recall: Failed Dissolution Specifications; product failed to meet 24-month stability
Failed Dissolution Specifications; product failed to meet 24-month stability testing acceptance criteria
-
Class II · 7 months ago
Apotex Corp. Brimonidine Tartrate/Timolol Maleate Ophthalmic Solution 0.2%/0.5%* recall: Lack of Assurance of Sterility
Lack of Assurance of Sterility
-
Class II · 1+ years ago
Apotex Corp. Brimonidine Tartrate/Timolol Maleate Ophthalmic Solution, 0.2%/0.5% recall: Lack of Assurance of Sterility; atypical weight loss due to improper bottle
Lack of Assurance of Sterility; atypical weight loss due to improper bottle sealing leading to potential sterility concerns
-
Class II · 1+ years ago
Apotex Corp. Ketorolac Tromethamine Ophthalmic Solution, 0.5%, 5 mL recall: Lack of Assurance of Sterility; atypical weight loss due to improper bottle
Lack of Assurance of Sterility; atypical weight loss due to improper bottle sealing leading to potential sterility concerns
-
Class II · 11 days ago
K.C. Pharmaceuticals, Inc. Sterile Lubricant Dry Eye Relief Eye Drops, 0.5 FL OZ recall: Lack of Assurance of Sterility
Lack of Assurance of Sterility