FDA recalls · F-1186-2019
ProThera, Inc. dba SFI USA recall
- FoodKlaire Labs Reduced L-Glutathione 150 mg capsules, single capsule dose 100 vegetarian capsules SKU V799-10 UPC Code: 7 09616 79910 9
- ReasonMis-packaging; product is labeled as Reduce L-Glutathione but actually contains Lithium Orotate.
- ClassClass II: the food could cause temporary or treatable health problems
- StatusClosed by FDA, ended 2019-04-02
- DatesFirm started it 2018-12-13. In FDA's enforcement report 2019-04-03.
- Sold inUS 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
- Amount139 bottles
- CodesFG Lot: 2018210303 Expiration: 05/2020
- FirmProThera, Inc. dba SFI USA, Reno, NV · Voluntary: Firm initiated
Products we list
None. We tie a recall to a product only by a barcode printed in the recall, and this one names none we list. That does not mean the recalled food is missing from our listings.
From FDA's enforcement report, via openFDA (CC0): raw data for this recall. FDA's own Enforcement Report search finds it by its number, F-1186-2019. Class meanings: FDA.