StellaLife VEGA Oral Care Spray Recalled for Bacillus Contamination
StellaLife VEGA Oral Care spray bottles have been recalled due to contamination with multiple Bacillus species organisms. The FDA Class I recall affects 31,811 bottles distributed nationwide to physician offices.
What this means for you
Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: This is an FDA Class I recall, which per the severity rubric establishes a minimum severity score of Severe. Bacillus species contamination in a non-sterile oral product presents a significant potential health hazard.
Plain-English summary
StellaLife VEGA Oral Care is a homeopathic oral spray containing multiple plant-based and mineral-derived ingredients, distributed as 1 fl oz bottles. The product has been recalled due to microbial contamination with multiple Bacillus species organisms detected in the non-sterile drug product.
The affected product is Lot #2552 with an expiration date of February 28, 2026. A total of 31,811 bottles have been distributed nationwide to 60 physician offices.
The FDA has classified this as a Class I recall. Consumers who have received this product should stop using it immediately and contact their healthcare provider or pharmacy for guidance on proper disposal or return.
The recalled product
- Product
- STELLALIFE VEGA ORAL CARE (ARNICA, CALENDULA, CHAMOMILLA, ECHINACEA ANGUSTIFOLIA, ECHINACEA PURPUREA, HEPAR SULPH CALC, HYPERICUM, LGNATIA, RUTA, STAPHYSAGRIA)
- Brand
- STELLALIFE VEGA ORAL CARE
- Manufacturer
- Homeocare Laboratories, Inc.
- Category
- Drug — Homeopathic Oral Care
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 (2)
- Lot # 2552
- exp. date 02-28-2026
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 2 recalled by Homeocare Laboratories, 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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