Fluticasone Propionate Nasal Spray — Class II drug recall D-1172-2022
Terminated recall by Akorn, Inc., reported 2022-07-06, distributed nationwide. Defective container: defect prevents product from dispensing as intended.
| Recall number | D-1172-2022 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Akorn, Inc., Lake Forest, IL, United States |
| Recall initiated | 2022-06-13 |
| Classified | 2022-06-30 |
| Reported by FDA | 2022-07-06 |
| Terminated | 2024-07-14 |
| Distributed | Nationwide (US) |
| Quantity | 44,400 bottles |
| Reason classes | packaging |
| NDC | 50383-0700-16 |
| Lot numbers | 379073, 379079 |
| Expiration dates | 2023-09-30 |
Product
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
Reason for recall
Defective container: defect prevents product from dispensing as intended.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-1172-2022. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.