Klaire Labs Reduced L-Glutathione 150 mg capsules, single capsule dose 100 vegetarian capsules SKU V799-10

Recall map → All recalls → F-1186-2019

Klaire Labs Reduced L-Glutathione 150 mg capsules, single capsule dose 100 vegetarian capsules SKU V799-10 UPC Code: 7 09616 79910 9 ProThera, Inc. dba SFI USA · reported 2019-04-03

Terminated This recall has been closed out by the agency.

Reason for recall: Mis-packaging; product is labeled as Reduce L-Glutathione but actually contains Lithium Orotate.
Classification: Class II
Recall initiated: 2018-12-13
Reported by the agency: 2019-04-03
Closed out (terminated): 2019-04-02
Recalling firm: ProThera, Inc. dba SFI USA
Reno, NV
United States
This is the firm that issued the recall — commonly a distributor or processor. It is not the origin of contamination.
Distribution (the agency's own words): 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
States we parsed from that text: AL AZ CA KS LA MI MO NH NJ NY OR PA TX WA
The agency named these states. Parse method explicit_state_list, confidence high.
Food category: Dietary supplementsderived
Assigned by a reviewed keyword rulebook over the product description, not by the agency.
Recall type: Voluntary: Firm initiated
Recall number: F-1186-2019

This page reproduces a record published by the US Food and Drug Administration. It is not real-time: recalls typically appear in FDA's Enforcement Report weeks after they begin — a median of 40 days, see publication lag. For current food safety information consult FDA and USDA FSIS directly.