The Recall Desk
Agency classClass IIOur severity:ModerateFDA (Drugs)·D-0890-2023·Announced 2023-07-05

Drug Oral Care Spray Recalled for Manufacturing Practice Deviations

StellaLife VEGA Oral Care Spray is being recalled for manufacturing deviations. The product was distributed nationwide; consumers should discontinue use of affected lots.

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: This is a voluntary precautionary recall due to manufacturing practice deviations with no reported illnesses or injuries. It meets the Moderate severity criterion for voluntary recalls without confirmed harm.

Plain-English summary

StellaLife VEGA Oral Care Spray (1 fl oz/30 ml tubes, peppermint flavor), manufactured by Homeocare Laboratories, Inc., is being recalled due to manufacturing practice deviations. The spray is an over-the-counter oral care product.

The product was distributed throughout the United States. Affected lots are #2407 (expiration February 2024), #2409A (expiration April 2024), and #2409B (expiration May 2024). A total of 33,109 tubes were distributed.

Consumers who have purchased this product should discontinue use immediately. The manufacturer voluntarily initiated the recall on June 5, 2023. For questions or to report adverse events, contact the manufacturer.

The recalled product

Product
STELLALIFE VEGA ORAL CARE (SPRAY)
Brand
STELLALIFE VEGA ORAL CARE
Manufacturer
Homeocare Laboratories, Inc.
Category
Drug — Oral Care
Hazard

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 (6)

  • Lot #2407
  • exp. date Feb-24
  • 2409A
  • exp. date Apr-24
  • 2409B
  • exp. date May-24

Distribution

Distributed nationwide across the United States.

Part of a larger recall action

This product is one of 11 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.

See all 11 products in this recall →

Related recalls

Same brand · STELLALIFE VEGA ORAL CARE

Same manufacturer · Homeocare Laboratories, Inc.

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Same hazard · manufacturing defect

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