Tatiomax — Class II drug recall D-1317-2014
Completed recall by Flawless Beauty LLC, reported 2014-05-21, distributed nationwide. Marketed Without An Approved NDA/ANDA: Product is sold over the counter whose labeling includes drug claims to
| Recall number | D-1317-2014 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Completed |
| Voluntary or mandated | Voluntary |
| Recalling firm | Flawless Beauty LLC, Asbury Park, NJ, United States |
| Recall initiated | 2014-04-29 |
| Classified | 2014-05-13 |
| Reported by FDA | 2014-05-21 |
| Distributed | Nationwide (US) |
| Reason classes | labeling, unapproved product |
| Lot numbers | UB302 |
| Expiration dates | 2015-05-12 |
Product
Tatiomax (reduced glutathione/hydrolyzed collagen) powder for injection vials, 1200 mg/200 mg, 10-count vials per box, Manufactured by: Sujie Pharmaceutical Ltd., Tokyo, Japan, UPC 4973430081576
Reason for recall
Marketed Without An Approved NDA/ANDA: Product is sold over the counter whose labeling includes drug claims to act as an antidote.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-1317-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.