CLASS II Drug recall · Reported 24 Jul 2024 · FDA Enforcement Report
Stellalife Advanced Formula Peppermint, Vega Oral Care, Rinse recalled
Homeocare Laboratories is recalling Stellalife Advanced Formula Peppermint, Vega Oral Care, Rinse, distributed nationwide in the US. The recall was initiated on 5 Jun 2024 and the FDA has classified it as Class II.
Check your package
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
- Recall number
- D-0610-2024
- FDA event ID
- 94782
- Recalling firm
- Homeocare Laboratories, Yonkers, NY
- Manufacturer
- StellaLife, Inc.
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 5 Jun 2024
- FDA classified
- 17 Jul 2024
- Reported
- 24 Jul 2024
- Type
- Voluntary: Firm initiated
- Customers notified by
- Press Release
- Reason category
- Sterility
Timeline
| 5 Jun 2024 | Recall initiated by company | |
| 17 Jul 2024 | Classified by FDA | +42 days |
| 24 Jul 2024 | Published in enforcement report | +7 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Microbial Contamination of Non-Sterile Products: presence of Terribacillus species organism
A sterility recall means a product that must be sterile, such as an injection or eye drop, may be contaminated. Using a non-sterile product can cause serious infection.
Product as listed by the FDA
STELLALIFE ADVANCED FORMULA Peppermint, VEGA Oral Care, Rinse, 16 fl oz (473 ml), Distributed by: StellaLife, 2875 NE 191 Street, Suite 500, Aventura, FL 33180, NDC 69685-143-16
Where it was distributed
Nationwide to 60 Physician offices
Questions about this recall
Why was it recalled?
Microbial Contamination of Non-Sterile Products: presence of Terribacillus species organism
Which lots are affected?
Lot # 2550, exp. date 02-28-2026
Where was it sold?
Nationwide to 60 Physician offices
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
More recalls from Homeocare Laboratories
All 12| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Kanjo Homeopathic Pain Relief Cream With Arnica recalled | Homeocare Laboratories | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | StellaLife VEGA Oral Care Gel tubes recalled by Homeocare Laboratories | Homeocare Laboratories | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | DoloEar Earache Drops recalled by Homeocare Laboratories | Homeocare Laboratories | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | StellaLife VEGA Oral Care Rinse, Peppermint recalledStellalife Vega Oral Care Rinse | Homeocare Laboratories | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | StellaLife VEGA Oral Care Spray recalled by Homeocare Laboratories | Homeocare Laboratories | Manufacturing (CGMP) Deviations | Nationwide |