FDA recall record

NutraCap Labs Revive MD Ashwagandha Capsules 60ct Bottle UPC CODE 7 28614 recall — FDA F-0484-2022

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

Class Iclassification
F-0484-2022official record ID
Jan 19, 2022report date

Recall record at a glance

Official recordF-0484-2022
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmNutraCap Labs LLC
Report dateJan 19, 2022
Recall initiation dateNov 9, 2021
Quantity80,169 various bottles and jars
LocationNorcross, GA, United States

Official product description

Revive MD Ashwagandha Capsules 60ct Bottle UPC CODE 7 28614 77933 3

Why the product was recalled

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

Distribution information

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.

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Press Release.

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.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

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