Food Recall Check
Class I · High risk Terminated Initiated Nov 9, 2021 (5 years ago)

Greater Her Resilient Capsules recall

Recalled by NutraCap Labs LLC · Norcross, GA, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

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

Undeclared allergen: Milk

For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.

What was recalled

Greater Her Resilient Capsules 30ct Bottle NO UPC CODE

Quantity: 80,169 various bottles and jars

Food: Dietary supplements

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 #2004251 EXP DATE 04/2022

Where it was sold

Alabama Arkansas Arizona California Colorado Connecticut Florida Georgia Idaho Illinois Indiana Kentucky Louisiana Maryland Minnesota North Carolina New Jersey Nevada New York Ohio Oregon South Carolina Tennessee Texas Virginia Washington

FDA's distribution note: 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.

Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. The risk from an undeclared allergen is to people allergic to milk; for anyone else the product is generally not a safety concern. 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
NutraCap Labs LLC
Initiated by
Voluntary: Firm initiated
Recall initiated
Nov 9, 2021
In FDA report of
Jan 19, 2022
Terminated
May 21, 2024
FDA recall number
F-0444-2022 · event 89000
Official record
FDA enforcement report search

Also recalled with it (105 more products)

FDA files each product of one recall action separately; these share the same FDA event.

Class II · Moderate risk Terminated Other

Raw Vegan Protein Peanut Butter

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

NutraCap Labs LLC 26 states F-0399-2022
Class I · High risk Terminated Undeclared milk

AIOS Synergy for Men Capsules

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

NutraCap Labs LLC 26 states F-0405-2022
Class I · High risk Terminated Undeclared milk

AIOS Synergy for Women Capsules

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

NutraCap Labs LLC 26 states F-0406-2022
Class I · High risk Terminated Undeclared milk

Alpha Woman Original Capsules

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

NutraCap Labs LLC 26 states F-0407-2022

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