E3 Artisan Recalls Blood Orange Meltaways Due to Undeclared Milk
E3 Artisan is recalling 40 bars of 3-piece Blood Orange Meltaways because FDA samples tested positive for undeclared milk.
The agency’s classification
FDA (Food): Class I
Class I is a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 4/5 (Severe).
The hazard poses a serious risk of illness, injury, or structural failure. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: The agency classified this as an FDA Class I recall, which mandates a severity score of at least 4 according to the rubric.
Plain-English summary
E3 Artisan is recalling 40 bars of 3-piece Blood Orange Meltaways. The recall was initiated because FDA samples of the product tested positive for milk, which was not declared on the product labels.
The affected product is identified by SKU ML1033 and has an expiration date range of 10/21/2015 to 1/15/2016. The firm distributed the product to 86 domestic firms.
Consumers with this product should stop using it and return it to the place of purchase or contact the manufacturer for further instructions.
The recalled product
- Product
- Meltaways- 3 piece Blood Orange meltaways.
- Manufacturer
- E3 Artisan
- Category
- Food — Chocolate Confectionery
- Affected units
- 40
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- SKU: ML1033 Expiration date range: 10/21/2015- 1/15/2016.
Distribution
Distribution scope not specified by the agency.
Part of a larger recall action
This product is one of 21 recalled by E3 Artisan under a single FDA (Food) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 21 products in this recall →Related recalls
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