CLASS II Food recall · Reported 27 May 2026 · FDA Enforcement Report

Liposomal D3+B12 Spray recalled by Wellnov Supplements

Wellnov Supplements is recalling Liposomal D3+B12 Spray, distributed nationwide in the US. The recall was initiated on 23 Apr 2026 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesDistribution Dates: 10/01/2024-04/08/2026 Lot Number DB1024 Expiry Date 10/2026
Quantity recalled23 bottles

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
H-0806-2026
FDA event ID
98832
Recalling firm
Wellnov Supplements, Chandler, AZ
Classification
Class II
Status
Terminated
Recall initiated
23 Apr 2026
FDA classified
19 May 2026
Reported
27 May 2026
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Lead & Heavy Metals
Product category
Vitamins

Timeline

23 Apr 2026Recall initiated by company
19 May 2026Classified by FDA+26 days
27 May 2026Published in enforcement report+8 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.

Lead and other heavy metals accumulate in the body. Children are most at risk; even low levels can affect development.

Product as listed by the FDA

Liposomal D3+B12 Spray. Dosage: 3 sprays Liquid. Packaging: Aluminum bottle. 30 ml. Firm Address: VitaminAlly LLC Chandler, AZ 85225.

Where it was distributed

Products were distributed nationwide and the United States Territory of Puerto Rico.

Nationwide Puerto Rico

Questions about this recall

Is Liposomal D3+B12 Spray recalled?

Yes. Wellnov Supplements recalled Liposomal D3+B12 Spray on 23 Apr 2026. The recall is Class II and its status is Terminated. Recall number H-0806-2026.

Why was it recalled?

Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.

Which lots are affected?

Distribution Dates: 10/01/2024-04/08/2026 Lot Number DB1024 Expiry Date 10/2026

Where was it sold?

Products were distributed nationwide and the United States Territory of Puerto Rico.

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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