ProThera, Inc. dba SFI USA — recall history

Every FDA and USDA recall we hold for ProThera, Inc. dba SFI USA. This is a record of published agency notices, not an assessment of the company: a recall is often the result of a firm's own testing and voluntary action, and firms that test more thoroughly may appear here more often.

Class IIIFDA17 Jan 2019KS

ProThera, Inc. dba SFI USA recalls Klaire Labs Melatonin Lozenge Formula Fast Dissolving 1 mg tablets; Packed in a 75 cc HDPE (Class III)

ProThera recalled Klaire Labs Melatonin Lozenge Formula tablets because some bottles were filled with L-Theanine instead of melatonin. Consumers expecting melatonin would receive a different supplement with different effects.

Brand: Klaire Labs

Class IIFDA13 Dec 2018AL, AZ, CA, KS +10

ProThera, Inc. dba SFI USA recalls Klaire Labs Reduced L-Glutathione 150 mg capsules, single capsule dose 100 vegetarian caps (Class II)

Klaire Labs Reduced L-Glutathione 150 mg capsules were mislabeled and actually contained Lithium Orotate instead. A person taking this product would receive an undeclared substance with different health effects than intended.

Brand: Klaire Labs