Recalls / Class I
Class ID-1467-2020
Class I— FDA's most serious classification, issued when there is a reasonable probability that use of or exposure to the drug will cause serious adverse health consequences or death.
Product
Recovery Releaf, Pure CBD Oil, Vanilla, 1000MG, 25MG per serving, 1 fl. oz (30 ml) bottles,Distributed by: Recovery Releaf, West Palm Beach, FL
- Affected lot / code info
- FG003133
Why it was recalled
Chemical contamination: product contains elevated levels of undeclared lead.
Recalling firm
- Firm
- MICHIGAN HERBAL REMEDIES
- Notification channel
- Type
- Voluntary: Firm initiated
- Address
- 904 Chicago Dr, Jenison, Michigan 49428-9351
Distribution
- Quantity
- 100 bottles
- Distribution pattern
- Nationwide via internet sales,retailers and distributors in the USA
Timeline
- Recall initiated
- 2020-06-18
- FDA classified
- 2020-08-04
- Posted by FDA
- 2020-08-12
- Status
- Completed
Source: openFDA Drug Enforcement endpoint. Recall record D-1467-2020. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.