MICHIGAN HERBAL REMEDIES recalls Pure CBD Oil Vanilla 1000MG bottles due to elevated lead levels. Consumers should stop using affected products immediately.
Chemical contamination: product contains elevated levels of undeclared lead.
MICHIGAN HERBAL REMEDIES is recalling Pure CBD Oil Vanilla 1000MG bottles because they contain unsafe levels of 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. Lead exposure is particularly dangerous for children and pregnant individuals as it can affect development and cause long-term health problems.
Anyone who owns or uses the recalled Pure CBD Oil Vanilla 1000MG bottles. Children and pregnant individuals are at higher risk due to lead exposure.
Look for Pure CBD Oil Vanilla 1000MG bottles labeled 1 fl. oz (30 ml). The product was distributed by Recovery Releaf in West Palm Beach, Florida.
Immediately stop using the recalled Pure CBD Oil Vanilla 1000MG bottles as they contain unsafe lead levels.
Lead is a toxic heavy metal that can cause serious health issues, especially for children and pregnant individuals. It can affect development and cause long-term health problems.
Check for Pure CBD Oil Vanilla 1000MG bottles labeled 1 fl. oz (30 ml). The product was distributed by Recovery Releaf in West Palm Beach, Florida.
Immediately stop using the product and contact the manufacturer for instructions on disposal or return.
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-1467-2020 — MICHIGAN HERBAL REMEDIES MICHIGAN HERBAL REMEDIES Hello, I own a MICHIGAN HERBAL REMEDIES that is covered by recall D-1467-2020 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.
