Agave Dream Lavender Recalled for Potential Listeria Contamination
Agave Dream is recalling 1 Pint Lavender products due to potential Listeria monocytogenes contamination. The product was distributed in eight U.S. states.
What this means for you
Highest-severity recall. Risk of serious injury or death is documented or strongly suspected. Stop using the product now and follow the agency's instructions.
Our severity reasoning: The recall is classified as FDA Class I, which meets the criteria for a Critical severity score (5) according to the rubric.
Plain-English summary
Agave Dream is recalling 8,094 cases of Agave Dream Lavender 1 Pint products (UPC Code 8 9934900206 2) due to potential Listeria monocytogenes contamination. The recall is classified as Class I by the U.S. Food and Drug Administration.
The affected products were distributed in the United States to California, Oregon, Illinois, Texas, Indiana, South Carolina, New Jersey, and Washington. There was no foreign distribution. The product code date is 12/2/17.
Consumers should check their pantries for this specific product and dispose of it or return it to the place of purchase. Listeria monocytogenes is a high-risk pathogen that can cause serious illness, particularly in vulnerable populations.
The recalled product
- Product
- Agave Dream Lavender 1 Pint UPC Code 8 9934900206 2
- Manufacturer
- Agave Dream
- Category
- Food — Beverage
- Hazard
- Affected units
- 8,094
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)
- Dates: 12/2/17
Distribution
Part of a larger recall action
This product is one of 5 recalled by Agave Dream 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.
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