CLASS II Drug recall · Reported 28 Feb 2024 · FDA Enforcement Report

Pure Care Foaming Mint Hand Sanitizer recalled by Alpha Aromatics

Alpha Aromatics is recalling Pure Care Foaming Mint Hand Sanitizer 62%, distributed in Michigan, North Carolina. The recall was initiated on 25 Jan 2024 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot # 2022-012884 Lot # 2023-002020 Lot # 2023-003532 Lot # 2023-003761
Quantity recalled676 gallons

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-0338-2024
FDA event ID
93880
Recalling firm
Alpha Aromatics, Pittsburgh, PA
Classification
Class II
Status
Terminated
Recall initiated
25 Jan 2024
FDA classified
16 Feb 2024
Reported
28 Feb 2024
Type
Voluntary: Firm initiated
Customers notified by
Letter
Drug class
Hand Sanitizer

Timeline

25 Jan 2024Recall initiated by company
16 Feb 2024Classified by FDA+22 days
28 Feb 2024Published in enforcement report+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

CGMP Deviations

Product as listed by the FDA

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.

Where it was distributed

Product was distributed to two accounts in NC and MI

MichiganNorth Carolina

Questions about this recall

Why was it recalled?

CGMP Deviations

Which lots are affected?

Lot # 2022-012884 Lot # 2023-002020 Lot # 2023-003532 Lot # 2023-003761

Where was it sold?

Product was distributed to two accounts in NC and MI

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.

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