CLASS I Drug recall · Reported 12 Oct 2022 · FDA Enforcement Report

Antica Farmacista Hand Sanitizer Ocean Citron recalled

Salon Technologies International is recalling Antica Farmacista Hand Sanitizer Ocean Citron (ethyl alcohol, denatured 65%), distributed in Florida, Washington. The recall was initiated on 14 Sep 2022 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot #: 1166A Exp. 6/18/2023
Quantity recalled512 bottles

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-0002-2023
FDA event ID
90874
Recalling firm
Salon Technologies International, Orlando, FL
Classification
Class I
Status
Terminated
Recall initiated
14 Sep 2022
FDA classified
4 Oct 2022
Reported
12 Oct 2022
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Benzene
Drug class
Hand Sanitizer

Timeline

14 Sep 2022Recall initiated by company
4 Oct 2022Classified by FDA+20 days
12 Oct 2022Published in enforcement report+8 days

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

Reason for recall

Chemical Contamination: product found to contain benzene

Product as listed by the FDA

Antica Farmacista Hand Sanitizer Ocean Citron (ethyl alcohol, denatured 65%) packaged in 473 mL/16 fl. oz. bottles, Dist. By Antica Farmacista Seattle, WA 98122 UPC 8 47005 00450 9

Where it was distributed

FL and WA only

FloridaWashington

Questions about this recall

Why was it recalled?

Chemical Contamination: product found to contain benzene

Which lots are affected?

Lot #: 1166A Exp. 6/18/2023

Where was it sold?

FL and WA only

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 I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

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.

Other products in this recall event

1 other product · FDA event 90874

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