Liposomal D3+B12 Spray — Class II food recall H-0806-2026
Terminated recall by Wellnov Supplements LLC, reported 2026-05-27, distributed nationwide. Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible
| Recall number | H-0806-2026 |
|---|---|
| Product type | Food |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Wellnov Supplements LLC, Chandler, AZ, United States |
| Recall initiated | 2026-04-23 |
| Classified | 2026-05-19 |
| Reported by FDA | 2026-05-27 |
| Terminated | 2026-07-10 |
| Distributed | Nationwide (US) |
| Quantity | 23 bottles |
| Reason classes | microbial contamination, cgmp |
| Pathogens | clostridium botulinum |
| Lot numbers | DB1024 |
| Expiration dates | 2026-10 |
Product
Liposomal D3+B12 Spray. Dosage: 3 sprays Liquid. Packaging: Aluminum bottle. 30 ml. Firm Address: VitaminAlly LLC Chandler, AZ 85225.
Reason for recall
Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/H-0806-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.