Recall · openFDA Food Enforcement

Xenesta Nuvive Womens 90 count packaged in a white plastic…: FDA Recall F-0915-2018

Agency action: Feb 23, 2018Record ID: F-0915-2018
View official source ↗

What happened

Original notice title

Xenesta Nuvive Womens 90 count packaged in a white plastic bottle with white cap, recall F-0915-2018

From the archived source record

Recalled dietary supplements may contain undeclared milk.

What the official notice says to do

Check the original notice for the instructions that apply to the named product, company, and affected lots.

Read the official notice →

Status and source details

Status recorded in the archive
Terminated
FDA recall classification
Class I
Recall initiated by
Voluntary: Firm initiated
Report date
Mar 21, 2018
Termination date in the archive
Aug 7, 2018
Source checked
Jul 16, 2026
Record revision
22829d071d32

This is a dated record. Its current status may have changed since the source was captured. A record applies to its stated scope; it is not a safety rating for every product from a company.

Sources, dates, and coverage →

What is affected

Product
Xenesta Nuvive Womens 90 count packaged in a white plastic bottle with white cap
Company
Progressive Laboratories, Inc
Lot / identifier
Lot # 2071957 and 2082387
Market / distribution
Nationwide through the United States