E3 Artisan recalls Blood Orange & Vanilla Bean Meltaway bars due to undeclared milk in FDA samples. Consumers should check labels for milk content.
Undeclared Milk on the labels of various dark chocolate bars. FDA samples came back positive for milk.
E3 Artisan is recalling Blood Orange & Vanilla Bean Meltaway chocolate bars because FDA tests found milk in the product. This is a food safety issue that could cause allergic reactions for people with milk allergies.
The bars contain undeclared milk, which can cause allergic reactions in people sensitive to dairy. FDA testing confirmed milk presence in samples, but the product is not intended to be consumed by those with milk allergies.
People who own or consume the recalled Meltaway bars are affected. Those with milk allergies are at higher risk due to the undeclared milk.
Check for the product name 'Meltaway bar- Blood Orange & Vanilla bean' on the label. The SKU is MB1023 with an expiration date between October 21, 2015, and January 15, 2016.
Look for the product name 'Meltaway bar- Blood Orange & Vanilla bean' and SKU MB1023 on the label.
FDA samples tested positive for milk, but the manufacturer did not declare milk as an ingredient.
This is a food safety issue for people with milk allergies, but it does not pose a risk of serious injury to the general public.
Check for the product name 'Meltaway bar- Blood Orange & Vanilla bean' and SKU MB1023 with an expiration date between October 21, 2015, and January 15, 2016.
We’ve drafted a message you can send E3 Artisan to request your refund or repair — edit it as you like.
Subject: Recall F-0314-2016 — E3 Artisan E3 Artisan Hello, I own a E3 Artisan that is covered by recall F-0314-2016 from E3 Artisan. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
