Check the Batch
Class ITerminated in FDA datasetRecall initiated Nov 9, 2021

UXO Supplements Ghillie Peach Mango 19oz Jar

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.

Check your package

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

ProductUXO Supplements Ghillie Peach Mango 19oz Jar UPC CODE 6 37230 58495 8
Package size19oz
UPC637230584958

FDA code information

LOT #20122166 EXP DATE 12/2022 LOT #2106169 EXP DATE 06/2023 LOT #2008030 EXP DATE 08/2022 LOT #2004049 EXP DATE 04/2022

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original product description

UXO Supplements Ghillie Peach Mango 19oz Jar UPC CODE 6 37230 58495 8

Extracted codes and context

TypeCode / valueContext
UPC637230584958UXO Supplements Ghillie Peach Mango 19oz Jar UPC CODE 6 37230 58495 8
lot2004049P DATE 12/2022 LOT #2106169 EXP DATE 06/2023 LOT #2008030 EXP DATE 08/2022 LOT #2004049 EXP DATE 04/2022
lot2008030LOT #20122166 EXP DATE 12/2022 LOT #2106169 EXP DATE 06/2023 LOT #2008030 EXP DATE 08/2022 LOT #2004049 EXP DATE 04/2022
lot20122166LOT #20122166 EXP DATE 12/2022 LOT #2106169 EXP DATE 06/2023 LOT #2008030 EXP DATE 08/2022 LOT #2004049 EXP DATE 04/2022
lot2106169LOT #20122166 EXP DATE 12/2022 LOT #2106169 EXP DATE 06/2023 LOT #2008030 EXP DATE 08/2022 LOT #2004049 EXP DATE 04/2022

Original FDA recall reason

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

Recall details

Recall number
F-0496-2022
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-0496-2022

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

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