FDA Drug recall D-0326-2018
Tatiomax Gluatathione Whitening kits, 1400mg vials, Made in Japan
- FDA Drug
- Class II
- terminated
- Published 2018-02-14
On 2018-02-14 the FDA classified a Class II recall of Tatiomax Gluatathione Whitening kits, 1400mg vials, Made in Japan by Flawless Beauty, citing marketed Without An Approved NDA/ANDA: Flawless Beauty, LLC is voluntarily recalling all lots of different products sold individually or as part of multi-unit kits in accordance w….
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0326-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-01-19 |
| Published | 2018-02-14 |
| Last updated | 2026-09-13 11:52 UTC |
| Company | Flawless Beauty |
| Distribution | US |
Product
Tatiomax Gluatathione Whitening kits, 1400mg vials, Made in Japan
Reason
Marketed Without An Approved NDA/ANDA: Flawless Beauty, LLC is voluntarily recalling all lots of different products sold individually or as part of multi-unit kits in accordance with Consent Decree of Permanent Injunction ordered by the United States District Court due to misbranding and unapproved new drugs pursuant to the FD&C Act.
Identifiers
| code_info | all lots |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0326-2018%22
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