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.
The agency’s classification
FDA (Food): Class I
Class I is a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 4/5 (Severe).
The hazard poses a serious risk of illness, injury, or structural failure. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: The agency classified this recall as Class I — a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death. On that classification alone this is scored Severe; a score of Critical is reserved for recalls where a death or serious injury was reported. The agency gives the reason as: "Recalled dietary supplements may contain undeclared milk."
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
- Manufacturer
- Progressive Laboratories, Inc
- Category
- Food — Dietary Supplement
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 →Related recalls
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