Food recall

Supplement Manufacturing Partner, Inc. recall: Havasu Beetroot Powder

Supplement Manufacturing Partner, Inc., of Edgewood, NY, recalled Havasu Beetroot Powder. The FDA's reason: “Contains undeclared milk.” The FDA classified it Class II: it could cause temporary or minor harm. The company began the recall voluntarily on June 12, 2023, and the FDA first listed it in its Enforcement Report of July 12, 2023. The FDA has closed the recall: it found the company did all it reasonably could to remove or correct the product.

How serious

Class II

It could cause temporary or minor harm

Why

Allergen not on the label

Status

Terminated

Closed June 26, 2024

The recall

Company
Supplement Manufacturing Partner, Inc. (Edgewood, NY)
Reason, in FDA's words
“Contains undeclared milk”
Where it was sold
Amazon nationwide; Shopify nationwide
Recall began
, by the company
FDA classified it
First in an FDA Enforcement Report
FDA event number
92507

The product recalled

As the FDA describes them, with the codes that tell whether a package is part of the recall.

  • F-1224-2023 Class II

    Havasu Beetroot Powder, 11.5 oz.

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

    Quantity: 1,501 units

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Source and notes

U.S. Food and Drug Administration, Enforcement Reports (openFDA food recall data) (Public domain (U.S. government work); source U.S. Food and Drug Administration, openFDA), data as of July 12, 2023.

Each week the FDA lists the recalls it has classified in its Enforcement Report, often weeks after the company announced the recall, so a month with five weekly reports tends to count more. Each recall counts once, however many products it covers, in the month FDA first listed it. Class I means the food could cause serious harm or death, Class II temporary or minor harm, and Class III is unlikely to harm anyone. Meat, poultry and most egg products are recalled by the U.S. Department of Agriculture, not the FDA, and aren't included. For what to do with a recalled product, see the FDA's recalls page.