StellaLife VEGA Oral Gel Rinse Recalled for CGMP Deviations
Washington Homeopathic Products, Inc. is recalling StellaLife VEGA Oral Gel Rinse because it was not manufactured under current good manufacturing practices.
The agency’s classification
FDA (Drugs): 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 2/5 (Moderate).
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II and involves CGMP deviations without reported illnesses or injuries, fitting the criteria for a moderate severity voluntary precautionary recall.
Plain-English summary
Washington Homeopathic Products, Inc. is recalling StellaLife VEGA Oral Gel Rinse, packaged in 1000 mL white plastic bottles. The product contains equal parts of Azadirachta Indica 1x, Calendula Officinalis 1x, Echinacea Purpurea 1x, and Plantago Major 1x.
The recall was initiated because the products were not manufactured under current good manufacturing practices (CGMP). The specific lot number is 29488.
The product was distributed nationwide throughout the United States, Canada, and Saudi Arabia. Consumers should stop using the product and contact the manufacturer for further instructions.
The recalled product
- Product
- StellaLife VEGA Oral Gel Rinse (In equal parts of: Azadirachta Indica 1x, Calendula Officinalis 1x, Echinacea Purpurea 1x, Plantago Major 1x), packaged in 1000 mL white plastic bottle.
- Manufacturer
- Washington Homeopathic Products, Inc.
- Category
- Drug — Homeopathic
- Hazard
- Affected units
- 1
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 # 29488
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 16 recalled by Washington Homeopathic Products, Inc. under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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