# FDA recall D-0050-2019

> **Product Quest Manufacturing LLC** · Class II · drug recall initiated 2018-08-03.

## Product

QC Quality Choice, Saline Nasal Relief, Moisturizing Nasal Spray, Sodium Chloride 0.65%, packaged as a) 1.5 FL OZ (45 mL) bottle UPC 6 35515 98845 3; b) 3 FL OZ (89 mL) bottle UPC 6 35515 95042 9, Distributed by C.D.M.A., Inc., 43157 W. Nine Mile, Novi, MI 48376-0995.

## Reason for recall

CGMP Deviations: products manufactured under conditions that could impact its product quality.

## Distribution

Nationwide in the USA

## Key facts

- **Recall number:** D-0050-2019
- **Recalling firm:** Product Quest Manufacturing LLC
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2018-08-03
- **Report date:** 2018-10-24
- **Termination date:** 2021-03-30

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Daytona Beach, FL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0050-2019

## Citation

> AI Analytics. FDA recall D-0050-2019. Retrieved 2026-07-08 from https://api.ai-analytics.org/recall/D-0050-2019. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*
