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Food FDA Class III Terminated Undeclared allergen

Instant Milk Tea Honeydew Flavor, R&M Refresher brand, B0D7269JC1, net wt. 1lb. Product was sold in 1-pack or 3-pack. Parent ASIN #B0D728CZWS 1-pack ASIN #B0D7269JC1 3-pack ASIN #B0D726K269 Label declares Ingredients: Non-Dairy Creamer (Glucose Syrup, Vegetable Oil, Whey Powder, Sodium Caseinate

R&M TRADING LLC Published Jun 18, 2025

Risk level

Class III

Unlikely to cause harm, but violates labeling or manufacturing rules.

Severity score 35/100

What should you do?

  • Check whether you have this product, using the lot codes, UPCs, and dates listed below.
  • If you are allergic or sensitive to the ingredient noted, do not eat it — it could cause a serious reaction.
  • Return it to the place of purchase for a refund, or throw it away in a sealed bag so people and animals can’t get to it.
  • Contact R&M TRADING LLC or your place of purchase with questions, and see the source record below for full details.
Reason for recall

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

Hazards

Milk · primary

Affected products (1)

Instant Milk Tea Honeydew Flavor, R&M Refresher brand, B0D7269JC1, net wt. 1lb. Product was sold in 1-pack or 3-pack. Parent ASIN #B0D728CZWS 1-pack ASIN #B0D7269JC1 3-pack ASIN #B0D726K269 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.

Firm did not provide

Code info: Expiration Date 12/15/2025

Affected areas

Nationwide

Timeline

  1. Initiated
    May 12, 2025
  2. Published
    Jun 18, 2025
  3. Terminated
    Feb 3, 2026
Recall number
F-0931-2025
Agency
U.S. Food and Drug Administration
Country
US
Source data (openFDA JSON) About FDA enforcement reports

FDA records come from the openFDA food enforcement-report dataset — the agency's full weekly enforcement list. Most entries are not issued as consumer press releases, so they won't appear on fda.gov/recalls or in a web search. The source record link above resolves this exact recall by its number.