Class ITerminated in FDA datasetRecall initiated Nov 9, 2021

Black Magic Brain Waves Capsules 120ct Bottle

Recalling firm: NutraCap Labs LLC

Why it was recalled

During an FDA investigation the firm was notified that the product contains undeclared milk.

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: May 21, 2024.

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Compare the exact product and package details with the label you have.

ProductBlack Magic Brain Waves Capsules 120ct Bottle UPC CODE 0 74647 77431 6

FDA code information

LOT #2109334 EXP DATE 09/2023 LOT #2105136 EXP DATE 05/2023 LOT #2010279 EXP DATE 10/2022 LOT #2008057 EXP DATE 08/2022 LOT #2005105 EXP DATE 05/2022

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Full FDA record and distribution details

Original product description

Black Magic Brain Waves Capsules 120ct Bottle UPC CODE 0 74647 77431 6

Extracted codes and context

TypeCode / valueContext
lot2005105P DATE 05/2023 LOT #2010279 EXP DATE 10/2022 LOT #2008057 EXP DATE 08/2022 LOT #2005105 EXP DATE 05/2022
lot2008057P DATE 09/2023 LOT #2105136 EXP DATE 05/2023 LOT #2010279 EXP DATE 10/2022 LOT #2008057 EXP DATE 08/2022 LOT #2005105 EXP DATE 05/2022
lot2010279LOT #2109334 EXP DATE 09/2023 LOT #2105136 EXP DATE 05/2023 LOT #2010279 EXP DATE 10/2022 LOT #2008057 EXP DATE 08/2022 LOT #2005105 EXP DATE 05/2022
lot2105136LOT #2109334 EXP DATE 09/2023 LOT #2105136 EXP DATE 05/2023 LOT #2010279 EXP DATE 10/2022 LOT #2008057 EXP DATE 08/2022 LOT #2005105 EXP DATE 05/2022
lot2109334LOT #2109334 EXP DATE 09/2023 LOT #2105136 EXP DATE 05/2023 LOT #2010279 EXP DATE 10/2022 LOT #2008057 EXP DATE 08/2022 LOT #2005105

Original FDA recall reason

During an FDA investigation the firm was notified that the product contains undeclared milk.

Recall details

Recall number
F-0417-2022
Event ID
89000
FDA status
Terminated
Initiated
Nov 9, 2021
Reported
Jan 19, 2022
Classified
Jan 11, 2022
Terminated
May 21, 2024
Quantity
80,169 various bottles and jars
Location
Norcross, GA, United States
Initiation type
Voluntary: Firm initiated
Notification
Press Release

Where it was distributed

Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, FL, GA, ID, IL, IN, KY, LA, MD, MN, NC, NJ, NV, NY, OH, OR, SC, TN, TX, VA & WA.

FDA source record · F-0417-2022

Data updated September 16, 2026. View official FDA data ↗

Follow official FDA and manufacturer guidance.