Class IITerminated in FDA datasetDec 13, 2018

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

Recalling firm: ProThera, Inc. dba SFI USA

Why it was recalled

Mis-packaging; product is labeled as Reduce L-Glutathione but actually contains Lithium Orotate.

Check the codes ↓

The exact product

Klaire Labs Reduced L-Glutathione 150 mg capsules, single capsule dose 100 vegetarian capsules SKU V799-10 UPC Code: 7 09616 79910 9

Check the codes

Compare these FDA-provided codes, lot numbers or dates with the product you have.

Match the product, size and code together. A similar name alone does not identify your batch.

Original FDA code information

FG Lot: 2018210303 Expiration: 05/2020

TypeCode / valueContext
UPC709616799109 capsules, single capsule dose 100 vegetarian capsules SKU V799-10 UPC Code: 7 09616 79910 9
lot2018210303FG Lot: 2018210303 Expiration: 05/2020

Recall details

Recall number
F-1186-2019
Event ID
81788
FDA status
Terminated
Initiated
Dec 13, 2018
Reported
Apr 3, 2019
Classified
Mar 22, 2019
Terminated
Apr 2, 2019
Quantity
139 bottles
Location
Reno, NV, United States
Initiation type
Voluntary: Firm initiated
Notification
Letter

Where it was distributed

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

FDA source record · F-1186-2019

Data updated September 16, 2026. View official FDA data ↗

A missing code match is not a guarantee of safety. Follow official FDA and manufacturer guidance.