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ProThera, Inc. dba SFI USA

ProThera, Inc. dba SFI USA Recalls

All product recalls associated with ProThera, Inc. dba SFI USA.

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Recall Summary

Total Recalls

Past Year

Class I (Serious)

Most Recent

Jan 2019

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 1–2 of 2 recalls

Melatonin Lozenges (Klaire Labs) – Incorrect filling (2019)

Small quantity of product labeled as Melatonin Lozenge Formula were filled with L-Theanine.

Class IIILow

FDAJan 17, 2019IN, KS• ProThera, Inc. dba SFI USA

L-Glutathione Capsules (ProThera) – Mis-packaging Issue (2018)

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

Class IIModerate

FDADec 13, 2018AL, AZ, CA +11 more• ProThera, Inc. dba SFI USA