Class ITerminated in FDA datasetRecall initiated Nov 9, 2021

ANTLS Supps Turmeric Capsules 120ct

Recalling firm: NutraCap Labs LLC

Why it was recalled

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

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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ProductANTLS Supps Turmeric Capsules 120ct UPC CODE "862995000454 862995000454

FDA code information

LOT #2101000 EXP DATE 01/2023 LOT #2105164 EXP DATE 05/2023

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Full FDA record and distribution details

Original product description

ANTLS Supps Turmeric Capsules 120ct UPC CODE "862995000454 862995000454

Extracted codes and context

TypeCode / valueContext
lot2101000LOT #2101000 EXP DATE 01/2023 LOT #2105164 EXP DATE 05/2023
lot2105164LOT #2101000 EXP DATE 01/2023 LOT #2105164 EXP DATE 05/2023

Original FDA recall reason

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

Recall details

Recall number
F-0409-2022
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-0409-2022

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

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