The Recall Desk
HighFDA (Food)·F-0915-2018·Announced 2018-03-21

Xenesta Nuvive Women's Supplement Recalled for Undeclared Milk

Progressive Laboratories is recalling Xenesta Nuvive Women's 90-count bottles due to potential undeclared milk content.

What this means for you

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

Our severity reasoning: The recall involves allergen mislabeling on a common allergen (milk), which corresponds to a severity score of 3 (High) according to the rubric, as no illnesses or injuries are explicitly reported in the source text.

Plain-English summary

Progressive Laboratories, Inc. is recalling Xenesta Nuvive Women's 90-count dietary supplements packaged in white plastic bottles with white caps. The recall involves 147 boxes, with two bottles per box, distributed nationwide in the United States. The specific lot numbers affected are 2071957 and 2082387.

The recall was initiated because the dietary supplements may contain undeclared milk. This is a significant safety concern for individuals with milk allergies or sensitivities, as the presence of an undeclared major allergen poses a risk of adverse health reactions.

Consumers who have purchased these specific lot numbers should stop using the product immediately. They should check their inventory for the lot numbers 2071957 and 2082387 and dispose of the product or contact the manufacturer for further instructions.

The recalled product

Product
Xenesta Nuvive Womens 90 count packaged in a white plastic bottle with white cap

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (1)

  • Lot # 2071957 and 2082387

Distribution

Distributed nationwide across the United States.

Part of a larger recall action

This product is one of 4 recalled by Progressive Laboratories, Inc under a single FDA (Food) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 4 products in this recall →