Reno, NV, United States
ProThera, Inc. dba SFI USA recalls
2 recalls recorded since 2018, most recently on 17 January 2019. None are listed as ongoing. Status and classification are as published by the FDA.
Recalls2
Ongoing (FDA)0
Terminated or completed2
Class I (FDA)0
Terminated Class III Food
- Recall started
- 17 January 2019
- Terminated
- 26 March 2019
- Reason
- Small quantity of product labeled as Melatonin Lozenge Formula were filled with L-Theanine.
- Distribution
- One customer in KS.
- Initiated
- Voluntary: Firm initiated
- Recall number
- F-1101-2019
- Klaire Labs Melatonin Lozenge Formula Fast Dissolving 1 mg tablets; Packed in a 75 cc HDPE Bottle 60 Tablets UPC: 8 28054 17845 8; SKU: ML1
Terminated Class II Food
- Recall started
- 13 December 2018
- Terminated
- 2 April 2019
- Reason
- Mis-packaging; product is labeled as Reduce L-Glutathione but actually contains Lithium Orotate.
- 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
- Initiated
- Voluntary: Firm initiated
- Recall number
- 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
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.