MICHIGAN HERBAL REMEDIES recalls CBD oil bottles with elevated lead levels. Consumers should stop using affected products due to chemical contamination risks.
Chemical contamination: product contains elevated levels of undeclared lead.
MICHIGAN HERBAL REMED: SP, hemp oil, Berry, and 300MG CBD products in 1 fl. oz bottles have been recalled because they contain elevated levels of undeclared lead. This contamination poses a health risk, especially for children and pregnant individuals.
The product contains elevated levels of lead, a toxic heavy metal that can cause serious health issues, particularly in children and pregnant individuals. Lead exposure can lead to developmental delays, neurological damage, and other health problems.
Anyone who owns or uses the recalled CBD oil bottles. Children and pregnant individuals are at higher risk due to lead exposure.
Check for bottles labeled 'SP, hemp oil, Berry, 300MG CBD, 1 FL. OZ (30 ML)' distributed by The Spiffy Piff. The product code FG003277 is also associated with this recall.
Immediately stop using the recalled CBD oil bottles as they contain elevated levels of lead.
Lead is a toxic heavy metal that can cause serious health issues, especially in children and pregnant individuals, including developmental delays and neurological damage.
Check for bottles labeled 'SP, hemp oil, Berry, 300MG CBD, 1 FL. OZ (30 ML)' distributed by The Spiffy Piff with product code FG003277.
The recall does not mention a fix; consumers must stop using the product immediately.
We’ve drafted a message you can send MICHIGAN HERBAL REMEDIES to request your refund or repair — edit it as you like.
Subject: Recall D-1465-2020 — MICHIGAN HERBAL REMEDIES MICHIGAN HERBAL REMEDIES Hello, I own a MICHIGAN HERBAL REMEDIES that is covered by recall D-1465-2020 from MICHIGAN HERBAL REMEDIES. 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.
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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.