Almond Milk Containing Real Milk Recalled In Texas, Elsewhere

AUSTIN, TX — More than 145,000 half-gallon of refrigerated almond milk distributed nationally, including in Texas, has been recalled because the product may contain actual milk — an undeclared allergen posing risks to those with severe sensitivity to dairy.

Massachusetts-based HP Hood LLC recalled its Vanilla Almond Breeze products after the discovery of cow milk was detected, according to the Food & Drug Administration. Regulators noted that the product is safe to drink unless the consumer has a milk allergy or sensitivity.

To date, there has been one report of an allergic reaction but medical treatment was not required, the FDA reported in the recall notice. However, the FDA noted people with milk allergies run the risk of serious and even life-threatening allergic reaction if the product is consumed.

All told, some 145,254 half-gallon cartons of the affected product were shipped to retailers and wholesalers in 28 states, including Texas. The recalled units represent less than 0.8 percent of half-gallon containers of refrigerated Vanilla Almond Breeze almond milk shipped by the company in the last twelve months, FDA officials said.

The recall only applies to the refrigerated Vanilla Almond Breeze almond milk with a use-by date of Sept. 2, 2018. To identify the affected product, consumers should look for the stamped information printed as:

• USE BY: SEP 02 18 (07:36 – 20:48) H5 L1 51-4109.
• USE BY: SEP 02 18 (07:36 – 20:48) H5 L2 51-4109.
• USE BY: SEP 02 18 (07:36 – 20:48) H6 L1 51-4109.
• USE BY: SEP 02 18 (07:36 – 20:48) H6 L2 51-4109.

Also, the product has a Universal Product Code (UPC bar code) of 41570 05621 on the side panel of the carton next to the nutrition facts.

Consumers who purchased the product may return it to the retail location where the purchase was made for a full refund or exchange, or visit http://www.bluediamond.comto complete a web form. Consumers with questions may contact Blue Diamond at 1-800-400-1522, Monday through Friday from 9 a.m. to 7 p.m. EST.

Below is a photo of the affected product and stamped information on the carton, as provided by the FDA:

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