Key Takeaway
"SUNDIAL***ETHIOPIAN ABISH (FENNUGREEK SEED POWDER.)***" by Sundial Herbal Products was recalled on June 30, 2020. The hazard: Recall required by Order of Permanent Injunction. The products are misbranded and deemed unapproved drugs based on labeling claims.
"SUNDIAL***ETHIOPIAN ABISH (FENNUGREEK SEED POWDER.)***"
Description
"SUNDIAL***ETHIOPIAN ABISH (FENNUGREEK SEED POWDER.)***"
Hazard / Reason
Recall required by Order of Permanent Injunction. The products are misbranded and deemed unapproved drugs based on labeling claims.
Class II: Product that may cause temporary or medically reversible health consequences.
Class II indicates the product may cause temporary or medically reversible health effects. The probability of serious harm is considered remote.
Products Affected
Company Information
Sundial Herbal Products
Bronx, NY, United States
View all 68 recalls by Sundial Herbal Products →Distribution
NY
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Frequently Asked Questions
Is this recall still active?
Check the status badge at the top of this page. "Ongoing" means the recall is still active and you should follow the remedy instructions. "Completed" or "Terminated" means the recall process has concluded, though the safety issue remains relevant for any unrepaired products.
How do I check if my product is affected?
Compare the model number, lot code, serial number, or date range listed in the recall notice with the information on your product's label or packaging. For vehicles, check your VIN at NHTSA.gov/Recalls.
What remedy is available for this recall?
Check the remedy section above or contact the manufacturer directly for current remedy options.
Where can I find the original recall notice?
This recall was issued by FDA Food. Visit the agency's official website for the original notice.