FDA Drug recall D-1318-2014
Saluta (reduced glutathione) Powder for Injection, 600 mg/vial, packaged in 10 vials per box, Exclusively Distributed by: QAF Pharmaceutica…
- FDA Drug
- Class II
- completed
- Published 2014-05-21
On 2014-05-21 the FDA classified a Class II recall of Saluta (reduced glutathione) Powder for Injection, 600 mg/vial, packaged in 10 vials per box, Exclusively Distributed by: QAF Pharmaceutica… by Flawless Beauty, citing marketed Without An Approved NDA/ANDA: Parenteral product is labeled for use as an antidote.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-1318-2014 |
| Classification | Class II |
| Status | completed |
| Initiated | 2014-04-29 |
| Published | 2014-05-21 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Flawless Beauty |
| Distribution | US |
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
Marketed Without An Approved NDA/ANDA: Parenteral product is labeled for use as an antidote.
Identifiers
| upc | 6920425209014 |
|---|---|
| code_info | Lot #: 201302275, Exp 01/20/15; 201308384, Exp 10/19/2015 |
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: completed.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1318-2014%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.