RECALLING FIRM / COMPANY
ProThera, Inc. dba SFI USA Recalls
Are there any recent recalls involving ProThera, Inc. dba SFI USA?
The FDA identifies this company as the recalling firm; this does not establish that it is the manufacturer, retailer or brand owner. “Recent ongoing” means initiated within 365 days of September 18, 2026, FDA status “Ongoing,” and no termination date. This snapshot cannot confirm what is active today.
2 FDA product recordsLatest initiation: Jan 17, 2019
Different batch.
Check the label.
Latest recalls involving ProThera, Inc. dba SFI USA
Most recently initiated in the available FDA data; these are not necessarily active recalls.
All recall records involving ProThera, Inc. dba SFI USA
Latest and historical records, ordered by initiation date (newest first). FDA status appears on each record.
Klaire Labs Melatonin Lozenge Formula Fast Dissolving 1 mg tablets; Packed in a 75 cc HDPE Bottle 60 Tablets
Small quantity of product labeled as Melatonin Lozenge Formula were filled with L-Theanine.
OtherView details →Klaire Labs Reduced L-Glutathione 150 mg capsules, single capsule dose 100 vegetarian capsules SKU V799-10
Mis-packaging; product is labeled as Reduce L-Glutathione but actually contains Lithium Orotate.
OtherView details →Found your product? Now check the codes.
Same product name. Different batch. Details matter.