Mylan Pharmaceuticals Inc. recalls Dymista (azelastine hydrochloride and fluticasone propionate) Nasal Spray, 137 mcg / 50 mcg per spray, packaged in a 23
Mylan recalls Dymista nasal spray due to potential glass fragments in bottles. This could cause injury if the glass breaks during use. Affected units were manufactured in India with specific lot numbers and expiration dates.
Use caution until it’s fixed
Presence of foreign substance: Potential for glass in the neck area of the glass bottles.
Contact the company & request your remedy
What happened, in plain English
Mylan is recalling Dymista nasal spray because glass fragments might be present in the bottle necks. This could lead to injury if the glass breaks during use. The recall affects specific lot numbers and expiration dates from India. Read more at govinfonow.com/recall/39852-mylan-dymista-nasal-spray-recall-potential-glass-in-bottles.
Source Summary by GovInfoNow · govinfonow.com/recall/39852-mylan-dymista-nasal-spray-recall-potential-glass-in-bottles · Updated October 6, 2026 · FDA enforcement record: FDA #D-1075-2018
Cite this page
“Mylan Dymista Nasal Spray Recall: Potential Glass in Bottles.” GovInfoNow, updated October 6, 2026. https://govinfonow.com/recall/39852-mylan-dymista-nasal-spray-recall-potential-glass-in-bottles. Based on FDA recall #D-1075-2018 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1075-2018%22&limit=1).
Why it’s dangerous
Glass fragments in the bottle necks could break during use, potentially causing injury to the nasal passages or face. This is a risk if the glass breaks while the spray is being used.
Who’s affected
People with prescriptions for Dymista nasal spray who received this specific product from India. Those using the spray regularly are at higher risk if glass fragments are present.
How to tell if you have this one
Check for the product name Dymista, 137 mcg / 50 mcg per spray, and the lot numbers GA70246 or GA70254. The expiration date is February 2019.
- Brand
Mylan- Category
Drug
What to do — step by step
Check Product Details
Look for the lot numbers GA70246 or GA70254 and expiration date February 2019 on the product label.
Questions people ask
Is this product safe to use?
The recall indicates potential glass fragments in the bottle necks, which could cause injury if the glass breaks during use. Do not use until you confirm it's safe.
What should I do if I have this product?
Check the product label for the lot numbers GA70246 or GA70254 and expiration date February 2019. If you have these, contact Mylan for instructions.
How can I tell if my product is affected?
The affected products were manufactured by Cipla Ltd. in India with specific lot numbers and expiration dates. Check the label for these details.
Contact Mylan
We’ve drafted a message you can send Mylan to request your refund or repair — edit it as you like.
Subject: Recall D-1075-2018 — Mylan Mylan Hello, I own a Mylan that is covered by recall D-1075-2018 from Mylan. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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-1075-2018 (July 25, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1075-2018 to see it in context.
- Plain-language summary written by qwen3:4b on October 6, 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.