Klaire Labs Reduced L-Glutathione 150 mg capsules — Class II food recall F-1186-2019
Terminated recall by ProThera, Inc. dba SFI USA, reported 2019-04-03, distributed in AL, AZ, CA, KS, LA, MI, MO, NH…. Mis-packaging; product is labeled as Reduce L-Glutathione but actually contains Lithium Orotate.
| Recall number | F-1186-2019 |
|---|---|
| Product type | Food |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | ProThera, Inc. dba SFI USA, Reno, NV, United States |
| Recall initiated | 2018-12-13 |
| Classified | 2019-03-22 |
| Reported by FDA | 2019-04-03 |
| Terminated | 2019-04-02 |
| Distributed | AL, AZ, CA, KS, LA, MI, MO, NH, NJ, NY, OR, PA, TX, WA |
| Countries outside the US | GB, KR, NL |
| Quantity | 139 bottles |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 00709616799109 |
| Lot numbers | 2018210303 |
| Expiration dates | 2020-05 |
Product
Klaire Labs Reduced L-Glutathione 150 mg capsules, single capsule dose 100 vegetarian capsules SKU V799-10 UPC Code: 7 09616 79910 9
Reason for recall
Mis-packaging; product is labeled as Reduce L-Glutathione but actually contains Lithium Orotate.
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/F-1186-2019. 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.