Pathway To Wellness CBD Oil Recalled for Undeclared Lead Contamination
Michigan Herbal Remedies is recalling 100 bottles of Pathway To Wellness CBD Oil due to elevated levels of undeclared lead. The product was sold nationwide via internet and retail channels.
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 rubric criteria for a Critical severity score (5) due to the reasonable probability of serious adverse health consequences.
Plain-English summary
Michigan Herbal Remedies is recalling 100 bottles of Pathway To Wellness, CBD Oil, Premium Hemp Oil Drops, Natural, 1000MG CBD, 1 FL OZ (30 ML). The recall is due to chemical contamination, specifically elevated levels of undeclared lead in the product.
The affected product, identified by code FG003151, was distributed nationwide via internet sales, retailers, and distributors in the USA. The recall is classified as Class I by the FDA, indicating a reasonable probability that use of the product will cause serious adverse health consequences or death.
Consumers who have purchased this product should stop using it immediately and contact the distributor or retailer for a refund or further instructions. Lead exposure can cause serious health issues, particularly in children and pregnant women.
The recalled product
- Product
- Pathway To Wellness, CBD Oil, Premium Hemp Oil Drops, Natural, 1000MG CBD, 1 FL OZ (30 ML) bottles, Distributed by: Pathway to Wellness
- Manufacturer
- MICHIGAN HERBAL REMEDIES
- Category
- Drug — CBD 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)
- FG003151
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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