US Drug Recall Register
Class II · Moderate risk Terminated Initiated Jun 13, 2022 (4 years ago)

Fluticasone Propionate Nasal Spray, USP, 50 mcg, 16 g net fill weight per amber glass…

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

Why it was recalled

Defective container: defect prevents product from dispensing as intended.

What was recalled

Fluticasone Propionate Nasal Spray, USP, 50 mcg, 16 g net fill weight per amber glass bottle, Rx only, Manufactured by: HI-TECH PHARMACAL CO., INC., Amityville, NY 11701. NDC 50383-700-16

Recalling firm
Akorn, Inc.
NDC code
50383-700-16
Origin
IL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1172-2022

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.

Other Fluticasone recalls

See all