HIGH RISK
Terminated
F-0915-2018
Xenesta Nuvive Womens 90 count packaged in a white plastic bottle with white cap
Recalled by Progressive Laboratories, Inc
Classification
Class I — Dangerous or defective products that predictably could cause serious health problems or death.
Reason for Recall
Recalled dietary supplements may contain undeclared milk.
Product Details
Product Quantity
147 boxes (2 bottles/box)
Product Type
Food
Code Info
Lot # 2071957 and 2082387
Voluntary/Mandated
Voluntary: Firm initiated
Distribution & Geography
Distribution Pattern
Nationwide through the United States
Company Location
Irving, TX, 75038-3514
Timeline
Report Date
03/21/2018
Recall Initiated
02/23/2018
Classification Date
03/13/2018
Termination Date
08/07/2018
Source: U.S. Food & Drug Administration (FDA) — FDA Recalls
Last updated: August 29, 2026
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