Agency classClass IIOur severity:High FDA (Food)·H-0807-2026·Announced 2026-05-27

VitaminAlly liposomal B12 spray recalled over manufacturing practice deviations

VitaminAlly Liposomal B12 Spray is being recalled over deviations from current Good Manufacturing Practices that could lead to bacterial pathogen 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

Liposomal B12 Spray, 30 ml in an aluminium bottle, from VitaminAlly LLC of Chandler, Arizona, is being recalled. The action covers 63 bottles.

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

The affected lot is MB1024, expiry 10/2026, distributed between 1 October 2024 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: Liposomal B12 Spray. Dosage: 3 sprays Liquid. Packaging: Aluminum bottle. 30 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: 63

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)

Distribution Dates: 10/01/2024-04/08/2026 Lot Number MB1024 Expiry Date 10/2026

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