The Recall Desk
ModerateFDA (Drugs)·D-0886-2023·Announced 2023-07-05

FDA Recalls StellaLife VEGA Oral Care Rinse for Manufacturing Deviations

The FDA is recalling StellaLife VEGA Oral Care Rinse nationwide due to current Good Manufacturing Practice (cGMP) deviations. The manufacturer voluntarily initiated the recall.

What this means for you

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: FDA Class II voluntary recall for manufacturing practice deviations with no specific contamination, illness, or injury reported in the source material.

Plain-English summary

StellaLife VEGA Oral Care Rinse (16 fl oz bottles, Peppermint flavor), manufactured by Homeocare Laboratories, Inc., is being recalled nationwide by the FDA. The product was distributed across the United States.

The recall was initiated due to current Good Manufacturing Practice (cGMP) deviations in the manufacturing process. This is a voluntary recall initiated by the manufacturer. The affected lot numbers and their expiration dates are: 2357B, 2333 (exp. Sep-2); 2367C, 2367D (exp. Nov-23); 2367E, 2367F (exp. Jan-24); 2395A, 2406 (exp. Feb-2); 2395B (exp. Mar-24); and 2395C (exp. Apr-24). Approximately 130,762 bottles were distributed.

If you have purchased this product, do not use it. Contact the manufacturer or your healthcare provider if you have questions. The recall was officially terminated on September 16, 2024.

The recalled product

Product
STELLALIFE VEGA ORAL CARE RINSE (RINSE)
Brand
STELLALIFE VEGA ORAL CARE RINSE
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 (16)

  • Lot # 2357B
  • 2333
  • exp. date Sep-2
  • 2367C
  • 2367D
  • exp. date Nov-23
  • 2367E
  • 2367F
  • exp. date Jan-24
  • 2395A
  • 2406
  • exp. date Feb-2
  • 2395B
  • exp. date Mar-24
  • 2395C
  • exp. date Apr-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 manufacturer · Homeocare Laboratories, Inc.

See all →

Same hazard · gmp deviation

See all →