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RECALL RECORD — CLASS IIRecall closedF-1186-2019/FDA enforcement
Prothera, INC. Dba Sfi USA·Food·Dec 13, 2018

Klaire Labs Reduced L-glutathione 150 mg Capsules, Single Capsule Dose 100 Vegetarian Capsules

What you need to know

Class II

  • What happened

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

  • Health risk

    The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. A safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

  • Action required

    Check the identifying codes below and stop using the product. Return it to the retailer for a refund or dispose of it safely, following the recall notice.

Recall closed · classified by the FDAAL, AZ, CA, KS +10 moreMore food

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Match before you discard

Product identification

Source: FDA FOOD

Brand nameProthera, INC. Dba Sfi USA
Recalling firmProthera, INC. Dba Sfi USAReno, NV, United States
UPC / barcodes
7 09616 79910 9
Lot / date codes
  • FG Lot: 2018210303 Expiration: 05/2020
Distribution area
ALAZCAKSLAMIMONHNJNYORPATXWA

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

United States

Quantity affected139 bottles
Recall initiationFDA report date: April 3, 2019
FDA recall numberF-1186-2019

Beyond the headline

The recall, in context

Prothera, INC. Dba Sfi USA initiated this food recall on December 13, 2018. The FDA enforcement report states: Mis-packaging; product is labeled as Reduce L-Glutathione but actually contains Lithium Orotate. The FDA report lists distribution as: 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.

The FDA enforcement report describes the reason as: Mis-packaging; product is labeled as Reduce L-Glutathione but actually contains Lithium Orotate.

Klaire Labs Reduced L-glutathione 150 mg Capsules, Single Capsule Dose 100 Vegetarian Capsules was made or distributed by Prothera, INC. Dba Sfi USA in Reno, NV, United States. This page reflects FDA report F-1186-2019, dated April 3, 2019.

Why this is a Class II recall

Class II means the product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. In this recall, a safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

FDA definition

The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote.

What to do now

  1. 1

    Stop using it

    Do not eat, drink or take the affected product.

  2. 2

    Check the codes

    Compare the UPC and lot code against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Product safety recall

Symptoms to watch for

The official enforcement report describes the specific risk. Follow the recall notice, check the product codes and do not use a product that may be affected.

Higher-risk groups

Children, pregnant people, older adults and people with weakened immune systems should take extra care when a product's safety is uncertain.

What to do now

  1. 1Stop using or eating the product and keep it away from children and pets.
  2. 2Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return.
  3. 3Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Read the official source record for the specific hazard and instructions.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the Klaire Labs Reduced L-glutathione 150 mg Capsules, Single Capsule Dose 100 Vegetarian Capsules recall?

Prothera, INC. Dba Sfi USA recalled Klaire Labs Reduced L-glutathione 150 mg Capsules, Single Capsule Dose 100 Vegetarian Capsules in an FDA Class II enforcement action reported as F-1186-2019. Mis-packaging; product is labeled as Reduce L-Glutathione but actually contains Lithium Orotate.

What should I do if I bought this product?

Check the identifying codes below and stop using the product. Return it to the retailer for a refund or dispose of it safely, following the recall notice. Stop using or eating the product and keep it away from children and pets. Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return. Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Is the Prothera, INC. Dba Sfi USA recall still active?

The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record F-1186-2019. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

Brand history

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Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.