Why it was recalled
Mis-packaging; product is labeled as Reduce L-Glutathione but actually contains Lithium Orotate.
Product description
Klaire Labs Reduced L-Glutathione 150 mg capsules, single capsule dose 100 vegetarian capsules SKU V799-10 UPC Code: 7 09616 79910 9
Lot numbers, UPCs & expiration codes
FG Lot: 2018210303 Expiration: 05/2020
Where it was sold
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
What to do if you have this product
- Compare the brand, size, and lot/UPC codes on your package with the codes above.
- If it matches, don't eat it. Return it to the store for a refund or throw it away.
- Wash surfaces and containers that touched the product.
- If you feel sick after eating it, contact your doctor. In an emergency call 911.
Recall details
- Recall number
- F-1186-2019
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- Dec 13, 2018
- FDA report date
- Apr 3, 2019
- Quantity
- 139 bottles
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- ProThera, Inc. dba SFI USA
Original FDA data
Every field from FDA enforcement report F-1186-2019, exactly as published.
Show all FDA fields
- City
- Reno
- State
- NV
- Status
- Terminated
- Country
- United States
- Event ID
- 81788
- Address
- 795 Trademark Dr
- Code information
- FG Lot: 2018210303 Expiration: 05/2020
- Postal code
- 89521-5920
- Report date
- Apr 3, 2019
- Product type
- Food
- Recall number
- F-1186-2019
- Classification
- Class II
- Recalling firm
- ProThera, Inc. dba SFI USA
- Product quantity
- 139 bottles
- Termination date
- Apr 2, 2019
- Reason for recall
- Mis-packaging; product is labeled as Reduce L-Glutathione but actually contains Lithium Orotate.
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- Klaire Labs Reduced L-Glutathione 150 mg capsules, single capsule dose 100 vegetarian capsules SKU V799-10 UPC Code: 7 09616 79910 9
- Distribution pattern
- 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
- Recall initiation date
- Dec 13, 2018
- Initial firm notification
- Letter
- Center classification date
- Mar 22, 2019