Home / ProThera, Inc. dba SFI USA / F-1186-2019
Class II
ProThera, Inc. dba SFI USA
Recall #F-1186-2019 · Initiated 2018-12-13
Plain-language summary
by FoodRecallsDB.infoWhat happened
ProThera, Inc. recalled 139 bottles of Klaire Labs Reduced L-Glutathione capsules because they were mislabeled—the bottles say they contain L-Glutathione but actually contain Lithium Orotate, a different supplement. This mix-up happened during packaging.
Who is at risk
Anyone who purchased this product is at risk, especially people taking medications or with health conditions that could be affected by lithium, since they would be taking an unexpected substance.
What to do
Check if you have this product by looking for SKU V799-10 or UPC 7 09616 79910 9 on the bottle. If you do, stop using it and contact ProThera, Inc. for a refund or replacement. If you've already taken some capsules and have concerns, consult your doctor.
Product
Klaire Labs Reduced L-Glutathione 150 mg capsules, single capsule dose 100 vegetarian capsules SKU V799-10 UPC Code: 7 09616 79910 9
Reason for recall
Mis-packaging; product is labeled as Reduce L-Glutathione but actually contains Lithium Orotate.
Quantity affected
139 bottles
Distribution
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
Lot / code info
FG Lot: 2018210303 Expiration: 05/2020
Voluntary / mandated
Voluntary: Firm initiated
Initial notification
Letter
Terminated
2019-04-02
Recalling firm
ProThera, Inc. dba SFI USA
795 Trademark Dr
Reno, NV 89521-5920
United States
Recall classification
Remote probability of serious adverse health consequences, or temporary reversible consequences.