# FDA recall D-1318-2014

> **Flawless Beauty LLC** · Class II · drug recall initiated 2014-04-29.

## Product

Saluta (reduced glutathione) Powder for Injection, 600 mg/vial, packaged in 10 vials per box, Exclusively Distributed by: QAF Pharmaceuticals Inc. Philippines, Unit Unit 202 ECG Building, Multinational Avenue, Multinational Village, Parahaque City, Metro Manila Philippines; Manufactured by: Shandong Luye Pharmaceutical Co. Ltd, Yantai Shandong, PRC la Luye Pharma Subsidiary,  UPC 6920425209014

## Reason for recall

Marketed Without An Approved NDA/ANDA: Parenteral product is labeled for use as an antidote.

## Distribution

Nationwide

## Key facts

- **Recall number:** D-1318-2014
- **Recalling firm:** Flawless Beauty LLC
- **Classification:** Class II
- **Product type:** drug
- **Status:** Completed
- **Initiation date:** 2014-04-29
- **Report date:** 2014-05-21

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Asbury Park, NJ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1318-2014

## Citation

> AI Analytics. FDA recall D-1318-2014. Retrieved 2026-06-23 from https://api.ai-analytics.org/recall/D-1318-2014. Source: US FDA. Licensed CC0.

---

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