Acadia Farms Serenity Hemp Oil Recalled for Undeclared Lead Contamination
Michigan Herbal Remedies is recalling Acadia Farms Serenity Hemp Oil bottles due to elevated levels of undeclared lead.
The agency’s classification
FDA (Drugs): 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 classification is FDA Class I, which mandates a minimum severity score of 4 according to the rubric.
Plain-English summary
Michigan Herbal Remedies is recalling 100 bottles of Acadia Farms, Serenity, soothing mint, 300 MG Hemp Oil, 1 Fl OZ (30 ML). The product was distributed nationwide via internet sales, retailers, and distributors in the USA.
The recall was issued because the product contains elevated levels of undeclared lead. The specific lot code associated with the recall is FG003177.
Consumers who have purchased this product should stop using it and contact the recalling firm for further instructions or a refund.
The recalled product
- Product
- Acadia Farms, Serenity, soothing mint, 300 MG Hemp Oil, 1 Fl OZ (30 ML) bottles, Distributed by: Acadia Farms, Rehobeth, Massachusetts
- Manufacturer
- MICHIGAN HERBAL REMEDIES
- Category
- Drug — Hemp Oil
- Affected units
- 100
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)
- FG003177
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 36 recalled by MICHIGAN HERBAL REMEDIES under a single FDA (Drugs) 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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