The Recall Desk
Agency classClass IOur severity:SevereFDA (Food)·F-0914-2018·Announced 2018-03-21

Xenesta Nuvive Men Supplement Recalled for Undeclared Milk

Progressive Laboratories is recalling Xenesta Nuvive Men dietary supplements because they may contain undeclared milk.

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 Men dietary supplements, 90-count bottles packaged in white plastic with white caps. The recall involves 88 boxes, with two bottles per box, distributed nationwide through the United States. The specific lot number is 2071887.

The recall was initiated because the recalled dietary supplements may contain undeclared milk. This poses a risk to consumers with milk allergies or sensitivities who may not be aware of the ingredient's presence.

Consumers who have purchased this product should stop using it immediately. They should check their inventory for the specific lot number 2071887 and contact the recalling firm or their point of purchase for instructions on how to return the product or obtain a refund.

The recalled product

Product
Xenesta Nuvive Mens 90 count packaged in an white plastic bottle with white cap
Manufacturer
Progressive Laboratories, Inc
Category
Food — Dietary Supplement
Hazard

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 # 2071887

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 →

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