FDA recall record

ProThera, Inc. dba SFI USA Klaire Labs Melatonin Lozenge Formula Fast Dissolving 1 mg recall — FDA F-1101-2019

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

Class IIIclassification
F-1101-2019official record ID
Mar 6, 2019report date

Recall record at a glance

Official recordF-1101-2019
CategoryFood Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmProThera, Inc. dba SFI USA
Report dateMar 6, 2019
Recall initiation dateJan 17, 2019
Quantity120 bottles
LocationReno, NV, United States

Official product description

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

Why the product was recalled

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

Distribution information

One customer in KS.

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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