RecallHawk
Class II Recall

Havasu Beetroot Powder, 11.5 oz.

Supplement Manufacturing Partner, Inc.

Summary

The FDA issued a Class II for Havasu Beetroot Powder, 11.5 oz. by Supplement Manufacturing Partner, Inc.. Reason: Contains undeclared milk.

Details

Source

Food Recall

External ID

F-1224-2023

Action Date

2023-07-12

Status

Terminated

Category

food

Product Description

Havasu Beetroot Powder, 11.5 oz.

Lot/Code Info: Lot # 111-2023021 and Best by date, January 2026 UPC: X002H69359

Quantity Affected: 1,501 units

Reason for Recall

Contains undeclared milk

Distribution

Amazon nationwide; Shopify nationwide

Type: Voluntary: Firm initiated

Recall Initiated: 2023-06-12

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 228 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Supplement Manufacturing Partner, Inc. has 2 FDA actions in our database, including 2 recalls.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Supplement Manufacturing Partner, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Supplement Manufacturing Partner, Inc. have FDA actions?

Supplement Manufacturing Partner, Inc. has 2 FDA actions in our database, including 2 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1224-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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