PlainRecalls
FDA Drug Moderate Class II Terminated

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

Reported: August 15, 2018 Initiated: July 25, 2018 #D-1075-2018

Product Description

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

Reason for Recall

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

Details

Units Affected
20,780 bottles
Distribution
U.S. Nationwide
Location
Morgantown, WV

Frequently Asked Questions

What product 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. Recalled by Mylan Pharmaceuticals Inc.. Units affected: 20,780 bottles.
Why was this product recalled?
Presence of foreign substance: Potential for glass in the neck area of the glass bottles.
Which agency issued this recall?
This recall was issued by the FDA Drug on August 15, 2018. Severity: Moderate. Recall number: D-1075-2018.