# FDA recall F-1186-2019

> **ProThera, Inc. dba SFI USA** · Class II · food recall initiated 2018-12-13.

## 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.

## Distribution

US distribution to the following: AL, AZ, CA, KS, LA, MI, MO, NH, NJ, NY, OR, PA, TX, and WA    Foreign distribution to the following: Netherlands, Great Britain, and Korea

## Key facts

- **Recall number:** F-1186-2019
- **Recalling firm:** ProThera, Inc. dba SFI USA
- **Classification:** Class II
- **Product type:** food
- **Status:** Terminated
- **Initiation date:** 2018-12-13
- **Report date:** 2019-04-03
- **Termination date:** 2019-04-02

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Reno, NV, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=F-1186-2019

## Citation

> MORVS. FDA recall F-1186-2019. Retrieved 2026-10-12 from https://api.morvs.ai/recall/F-1186-2019. Source: US FDA. Licensed CC0.

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