# FDA recall D-1172-2022

> **Akorn, Inc.** · Class II · drug recall initiated 2022-06-13.

## 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.

## Distribution

Nationwide USA

## Key facts

- **Recall number:** D-1172-2022
- **Recalling firm:** Akorn, Inc.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2022-06-13
- **Report date:** 2022-07-06
- **Termination date:** 2024-07-14

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Lake Forest, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1172-2022

## Citation

> AI Analytics. FDA recall D-1172-2022. Retrieved 2026-07-13 from https://api.ai-analytics.org/recall/D-1172-2022. Source: US FDA. Licensed CC0.

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