US Drug Recall Register
Class II · Moderate risk Terminated Initiated Jul 25, 2018 (8 years ago)

Dymista (azelastine hydrochloride and fluticasone propionate) Nasal Spray, 137 mcg / 50…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Presence of foreign substance: Potential for glass in the neck area of the glass bottles.

What was recalled

Dymista (azelastine hydrochloride and fluticasone propionate) Nasal Spray, 137 mcg / 50 mcg per spray, packaged in a 23 g net fill weight, Rx only, Manufactured by: Cipla Ltd., Goa, India, M.L.,, NDC 0037-0245-23

Recalling firm
Mylan Pharmaceuticals Inc.
NDC code
0037-0245-23
Origin
WV, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1075-2018

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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