Agency classClass IIOur severity:High FDA (Food)·H-0795-2026·Announced 2026-05-27

VitaminAlly Joint Nourish liquid recalled over manufacturing practice deviations

VitaminAlly Joint Nourish oral liquid is being recalled over deviations from current Good Manufacturing Practices that could lead to bacterial pathogen contamination and possible C. botulinum concerns.

The agency’s classification

FDA (Food): Class II

Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.

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 3/5 (High).

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: FDA Class II recall where the manufacturing deviations are described as potentially leading to bacterial pathogen contamination, a named risk of harm with no illnesses reported.

Plain-English summary

Joint Nourish, an oral liquid supplied in a 480 ml plastic bottle with a 2 tablespoon (30 ml) dose, from VitaminAlly LLC of Chandler, Arizona, is being recalled. The action covers 90 bottles.

The stated reason is deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen contamination and possible C. botulinum concerns. The FDA classified the action as Class II.

The affected lot is JN0925, expiry 09/2027, distributed between 1 October 2025 and 8 April 2026. Distribution was nationwide and to Puerto Rico.

Consumers who have the affected lot should stop using it and dispose of it or return it to the place of purchase. Anyone who has used it and feels unwell should contact a healthcare provider.

The recalled product

Product: Joint Nourish. Dosage:2 tablespoons (30mL). Liquid. For Oral use. Packaging: Plastic Bottle. Net Volume:480 ml. Firm Address: VitaminAlly LLC Chandler, AZ 85225.
Manufacturer: Wellnov Supplements LLC
Category: Food — Dietary supplement
Hazard: cgmp-deviation
bacterial-pathogen
clostridium-botulinum
class-ii
Affected units: 90

Distribution

Distributed nationwide across the United States.

The notice also names 1 state specifically:

Part of a larger recall action

This product is one of 14 recalled by Wellnov Supplements LLC 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 14 products in this recall →

Same manufacturer · Wellnov Supplements LLC

See all →

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Same hazard · cgmp deviation