Food Recall Check
Class II · Moderate risk Terminated Initiated Apr 8, 2021 (5 years ago)

Natrol Melatonin 3 mg recall

Recalled by Natrol, LLC · Chatsworth, CA, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

One lot of ALA 300 mg Cap-50 were labeled at Melatonin 3 mg Tab-60.

A label that does not match the product can hide an ingredient someone must avoid, or show a wrong use-by date. All labeling errors recalls.

What was recalled

Natrol Melatonin 3 mg, Tab 60 White bottle with purple flip-top cap. Fall asleep faster, Stay asleep longer, 100$ Drug Free 1 Tablet 20 minutes before bedtime. Manufactured by Natrol LLC. Chatsworth, CA 91311 USA

Quantity: 12,740 units

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

Lot 2084395, Expiration DEC31 23

Where it was sold

Alabama Arizona California Colorado Delaware Florida Georgia Iowa Illinois Indiana Kentucky Louisiana Massachusetts Maryland Maine Michigan Minnesota Missouri Mississippi North Carolina North Dakota New Jersey Nevada New York Ohio Oklahoma Oregon Pennsylvania Puerto Rico Tennessee Texas Utah Virginia Washington Wisconsin West Virginia

FDA's distribution note: AL, AZ, CA, CO, DE, FL, GA, IA, IL, IN, KY, LA, MA, MD, ME, MI, MN, MO, MS, NC, ND, NJ, NV, NY, OH, OK, OR, PA, PR, TN, TX, UT, VA, WA, WI, WV and Ukraine, Serbia, Italy, Trinidad, Croatia

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Natrol, LLC
Initiated by
Voluntary: Firm initiated
Recall initiated
Apr 8, 2021
In FDA report of
May 12, 2021
Terminated
Sep 20, 2021
FDA recall number
F-0479-2021 · event 87704
Official record
FDA enforcement report search