Key Takeaway
Xenesta Nuvive Womens 90 count packaged in a white plastic bottle with white cap by Progressive Laboratories, Inc was recalled on February 23, 2018. The hazard: Recalled dietary supplements may contain undeclared milk.
Xenesta Nuvive Womens 90 count packaged in a white plastic bottle with white cap
Description
Xenesta Nuvive Womens 90 count packaged in a white plastic bottle with white cap
Hazard / Reason
Recalled dietary supplements may contain undeclared milk.
Class I: Dangerous or defective product that could cause serious health problems or death.
Class I is the most serious recall classification used by the FDA, indicating a reasonable probability of serious health consequences or death.
Products Affected
Company Information
Progressive Laboratories, Inc
Irving, TX, United States
View all 4 recalls by Progressive Laboratories, Inc →Distribution
Nationwide through the United States
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Xenesta Nuvive Mens 90 count packaged in an white plastic bottle with white cap
February 23, 2018
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.