Use caution Drug recall · FDA · Published September 24, 2024

Glenmark Recalls Ryaltris Nasal Spray Due to Clogged Dip Tube

Glenmark Pharmaceuticals recalls specific lots of Ryaltris nasal spray because the dip tube may be clogged, preventing the medication from dispensing.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #D-0006-2025Drug Glenmark ›

Use caution until it’s fixed

Defective Delivery System: The dip tube is clogged causing the spray not to work.

Take action

Contact the company

Recalling firmGlenmark Pharmaceuticals Inc., USA750 Corporate Dr · Mahwah, NJ 07430-2009

✎ GovInfoNow plain-language explainer

Glenmark Pharmaceuticals Inc. is recalling Ryaltris (olopatadine hydrochloride and mometasone fluorate) Nasal Spray because the delivery system may be defective. Specifically, the dip tube inside the bottle can become clogged, which causes the spray to stop working. This means users might not receive their prescribed dose of medication. Read more at govinfonow.com/recall/32536-glenmark-recalls-ryaltris-nasal-spray-due-to-clogged-dip-tube.

Source Summary by GovInfoNow · govinfonow.com/recall/32536-glenmark-recalls-ryaltris-nasal-spray-due-to-clogged-dip-tube · Updated October 9, 2026 · FDA enforcement record: FDA #D-0006-2025

Cite this page

“Glenmark Recalls Ryaltris Nasal Spray Due to Clogged Dip Tube.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/32536-glenmark-recalls-ryaltris-nasal-spray-due-to-clogged-dip-tube. Based on FDA recall #D-0006-2025 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0006-2025%22&limit=1).

The FDA announced on Sept. 24, 2024, that Glenmark Pharmaceuticals Inc., USA voluntarily recalled Ryaltris Nasal Spray due to a defective delivery system. The dip tube may be clogged, causing the spray not to work. Owners should contact Hikma Specialty USA Inc. for a refund.

How to tell if you have it

Brand: Glenmark
Product: Ryaltris Nasal Spray
NDC: 59467-700-27
Lot codes: 14230425, 14240024, 14240029, 14240076, 14240082, 14240090, 14240100
Expiration dates: Nov-25, Dec-25, Jan-26
Quantity: 45,504 bottles

The hazard

The recall involves a defective delivery system where the dip tube is clogged, causing the spray not to work. According to the FDA, this defect prevents the proper delivery of the medication.

Context

GovInfoNow's records show Glenmark Pharmaceuticals Inc., USA has 54 other recalls on record since 2017-11-20. Other recent recalls of similar products include Apotex Desmopressin Nasal Spray Recall (2026-04-08), Walgreens Saline Nasal Spray with Xylitol Recall (2025-11-12), and Keystone Burkhart Anesthetic Gel Recall (2026-05-21).

How to tell if you have this one

Check your bottle for the brand name Ryaltris and the NDC number 59467-700-27. Verify if your lot number is one of the following: 14230425, 14240024, 14240029, 14240076, 14240082, 14240090, or 14240100. The bottles contain 240 metered sprays and were distributed nationwide in the USA.

Brand
Glenmark
Category
Drug

Based on the official FDA remedy

What to do — step by step

Check Your Bottle
Look at the label to confirm if your product matches the recalled NDC 59467-700-27 and one of the specific lot numbers listed in the recall.
Contact Your Pharmacist
If you have a recalled bottle, contact your pharmacist or healthcare provider to discuss obtaining a replacement or alternative treatment.

Where it went and when

Where it was distributed

Distributed nationwide.

FDA distribution: “Nationwide in the USA” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA published this recall 15 days after the firm started it.

Sep 24, 2024Firm started the recall
Oct 3, 2024FDA classified it Class II
Oct 9, 2024Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

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Other Glenmark recalls

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Keep exploring

Link to this recall

<a href="https://govinfonow.com/recall/32536-glenmark-recalls-ryaltris-nasal-spray-due-to-clogged-dip-tube">Glenmark Recalls Ryaltris Nasal Spray Due to Clogged Dip Tube (GovInfoNow)</a>

Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

Official source: FDA Recall #D-0006-2025 (September 24, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0006-2025 to see it in context.
Plain-language summary written by qwen3.6:35b-a3b on October 9, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.