RecallHawk
Class III Recall

Instant Milk Tea Matcha Flavor, R&M Refresher brand, B0D71Y85TG, net wt. 1lb. Product was sold in 1-pack or 3-pack. Par

R&M TRADING LLC

Summary

The FDA issued a Class III for Instant Milk Tea Matcha Flavor, R&M Refresher brand, B0D71Y85TG, net wt. 1lb. Pr by R&M TRADING LLC. Reason: The Instant Milk Tea Powder's ingredients statement declares Non-Dairy Creamer (Whey Powder, Sodium Caseinate) but does not specify milk..

Details

Source

Food Recall

External ID

F-0933-2025

Action Date

2025-06-18

Status

Terminated

Category

food

Product Description

Instant Milk Tea Matcha Flavor, R&M Refresher brand, B0D71Y85TG, net wt. 1lb. Product was sold in 1-pack or 3-pack. Parent ASIN #B0D728CZWS 1-pack ASIN #B0D71Y85TG 3-pack ASIN #B0D71YBV1X Label declares Ingredients: Non-Dairy Creamer (Glucose Syrup, Vegetable Oil, Whey Powder, Sodium Caseinate***). Product of China. Distributor: R&M Trading LLC Lakewood, WA 98499.

Lot/Code Info: Expiration Date 12/15/2025

Quantity Affected: Firm did not provide

Reason for Recall

The Instant Milk Tea Powder's ingredients statement declares Non-Dairy Creamer (Whey Powder, Sodium Caseinate) but does not specify milk.

Distribution

Nationwide

Type: Voluntary: Firm initiated

Recall Initiated: 2025-05-12

Company

R&M TRADING LLC

Bellevue, WA

Context & Analysis

This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.

This was one of 161 food recalls issued in the same week, part of 204 food-related FDA actions this month.

R&M TRADING LLC has 5 FDA actions in our database, including 5 recalls.

Frequently Asked Questions

What is a Class III recall?

A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.

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 (R&M TRADING LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does R&M TRADING LLC have FDA actions?

R&M TRADING LLC has 5 FDA actions in our database, including 5 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0933-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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