STELLALIFE ADVANCED FORMULA Peppermint recall
FDA recall D-0610-2024 · initiated Jun 5, 2024
Homeocare Laboratories, Inc. recalled STELLALIFE ADVANCED FORMULA Peppermint in Jun 2024 — an FDA Class II recall (D-0610-2024) because Microbial Contamination of Non-Sterile Products: presence of Terribacillus species organism.
May cause temporary or medically reversible harm; low probability of serious harm.
Why it was recalled
Microbial Contamination of Non-Sterile Products: presence of Terribacillus species organism
Sterility could not be assured
The maker could not guarantee the product was sterile. That matters most for injections and eye products, where a contaminated dose reaches past the body's defences.
This is a manufacturing or quality failure, not a finding that the medicine is unsafe to take — across every recall we hold, none was issued for that reason. It does not mean the batch was harmless.
Is your product affected? Check the lot number
A recall covers only specific lots. Find the lot number and expiration date on your package and compare them to the affected codes below — if yours is not listed, it was not part of this recall.
Quantity recalled: 31,110 x 16 fl. oz. bottle
Details
- Product
- 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
- Recalling company
- Homeocare Laboratories, Inc.
- Classification
- Class II
- Status
- Terminated
- Type
- Voluntary: Firm initiated
- Distribution
- Nationwide to 60 Physician offices
- Initiated
- Jun 5, 2024
- FDA report date
- Jul 24, 2024
Frequently asked
- Was STELLALIFE ADVANCED FORMULA Peppermint recalled?
- Homeocare Laboratories, Inc. recalled STELLALIFE ADVANCED FORMULA Peppermint in Jun 2024 — an FDA Class II recall (D-0610-2024) because Microbial Contamination of Non-Sterile Products: presence of Terribacillus species organism. May cause temporary or medically reversible harm; low probability of serious harm.
- Why was STELLALIFE ADVANCED FORMULA Peppermint recalled?
- Per the FDA enforcement record, the reason for recall D-0610-2024 was: Microbial Contamination of Non-Sterile Products: presence of Terribacillus species organism
- Is a recalled STELLALIFE ADVANCED FORMULA Peppermint dangerous to take?
- An FDA recall removes specific lots from the market for a defined reason and does not by itself mean the medicine is unsafe for everyone — your specific lot may never have been affected. May cause temporary or medically reversible harm; low probability of serious harm. Check the FDA notice for the affected lot numbers and expiration dates, and ask your pharmacist or doctor before stopping a prescribed medicine. This reproduces public FDA data and is not medical advice.
- Which lots of STELLALIFE ADVANCED FORMULA Peppermint are affected?
- Distributed: Nationwide to 60 Physician offices. The recall covers these lots — Lot # 2550, exp. date 02-28-2026. Check the lot number and expiration date on your package against this list; if yours is not listed, it was not part of recall D-0610-2024.