Pure Care Foaming Mint Hand Sanitizer 62% recall
FDA recall D-0338-2024 · initiated Jan 25, 2024
Alpha Aromatics recalled Pure Care Foaming Mint Hand Sanitizer 62% in Jan 2024 — an FDA Class II recall (D-0338-2024) because CGMP Deviations.
May cause temporary or medically reversible harm; low probability of serious harm.
Why it was recalled
CGMP Deviations
The manufacturing process itself
The FDA found the process itself out of compliance, usually before any defective product was identified.
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: 676 gallons
Details
- Product
- Pure Care Foaming Mint Hand Sanitizer 62%, Distributed by: Air Scent International, 290 Alpha Drive, RIDC Industrial Park, Pittsburg, PA 15238 USA, www.airscent.com, NDC 75009-562.
- Recalling company
- Alpha Aromatics
- Classification
- Class II
- Status
- Terminated
- Type
- Voluntary: Firm initiated
- Distribution
- Product was distributed to two accounts in NC and MI
- Initiated
- Jan 25, 2024
- FDA report date
- Feb 28, 2024
Frequently asked
- Was Pure Care Foaming Mint Hand Sanitizer 62% recalled?
- Alpha Aromatics recalled Pure Care Foaming Mint Hand Sanitizer 62% in Jan 2024 — an FDA Class II recall (D-0338-2024) because CGMP Deviations. May cause temporary or medically reversible harm; low probability of serious harm.
- Why was Pure Care Foaming Mint Hand Sanitizer 62% recalled?
- Per the FDA enforcement record, the reason for recall D-0338-2024 was: CGMP Deviations
- Is a recalled Pure Care Foaming Mint Hand Sanitizer 62% 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 Pure Care Foaming Mint Hand Sanitizer 62% are affected?
- Distributed: Product was distributed to two accounts in NC and MI. The recall covers these lots — Lot # 2022-012884 Lot # 2023-002020 Lot # 2023-003532 Lot # 2023-003761. 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-0338-2024.