Food Recall Check
Class II · Moderate risk Terminated Initiated Jun 12, 2023 (3 years ago)

Havasu Beetroot Powder recall

Recalled by Supplement Manufacturing Partner, Inc. · Edgewood, NY, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

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

Havasu Beetroot Powder, 11.5 oz.

Quantity: 1,501 units

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 # 111-2023021 and Best by date, January 2026 UPC: X002H69359

Where it was sold

Nationwide.

FDA's distribution note: Amazon nationwide; Shopify nationwide

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. 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
Supplement Manufacturing Partner, Inc.
Initiated by
Voluntary: Firm initiated
Recall initiated
Jun 12, 2023
In FDA report of
Jul 12, 2023
Terminated
Jun 26, 2024
FDA recall number
F-1224-2023 · event 92507
Official record
FDA enforcement report search

Other recalls by Supplement Manufacturing Partner, Inc.