The Recall Desk
Agency classClass IIOur severity:HighFDA (Food)·F-1224-2023·Announced 2023-07-12

Havasu Beetroot Powder Recalled for Undeclared Milk Allergen

Havasu Beetroot Powder (11.5 oz.) is being recalled because it contains undeclared milk. Consumers with milk allergies who consume this product may experience allergic reactions.

The agency’s classification

FDA (Food): Class II

Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.

This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work

What this means for you

Our assessment, not the agency’s: severity 3/5 (High).

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

Our severity reasoning: This is an FDA Class II recall for allergen mislabeling (undeclared milk, a common allergen). No illnesses or hospitalizations are reported in the source text. Per the rubric, allergen mislabeling on common allergens scores 3 (High).

Plain-English summary

Supplement Manufacturing Partner, Inc. is recalling Havasu Beetroot Powder (11.5 oz.) due to the presence of undeclared milk. Milk is a common food allergen, and consumers with milk allergies could experience allergic reactions if they consume this product.

The affected product was distributed nationwide through Amazon and Shopify. The recalled lot includes Lot #111-2023021 with a best-by date of January 2026 (UPC: X002H69359). Approximately 1,501 units are subject to this recall.

Consumers who have purchased this product and have a milk allergy should discontinue use immediately and dispose of the product safely. Anyone who has consumed this product and experiences symptoms of an allergic reaction should seek medical attention.

The recalled product

Product
Havasu Beetroot Powder, 11.5 oz.
Affected units
1,501

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (2)

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

Distribution

Distributed nationwide across the United States.

Same manufacturer · Supplement Manufacturing Partner, Inc.

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