Antica Farmacista Hand Sanitizer Ocean Citron (ethyl alcohol, denatured 65%) packaged in 473 mL/16 fl. oz. bottles, Dis
Summary
The FDA issued a Class I for Antica Farmacista Hand Sanitizer Ocean Citron (ethyl alcohol, denatured 65%) pac by Salon Technologies International Inc. Reason: Chemical Contamination: product found to contain benzene.
Details
Source
Drug Recall
External ID
D-0002-2023
Action Date
2022-10-12
Status
Terminated
Category
drug
Product Description
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
Lot/Code Info: Lot #: 1166A Exp. 6/18/2023
Quantity Affected: 512 bottles
Reason for Recall
Chemical Contamination: product found to contain benzene
Distribution
FL and WA only
Type: Voluntary: Firm initiated
Recall Initiated: 2022-09-14
Company
Orlando, FL
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 33 drug recalls issued in the same week, part of 267 drug-related FDA actions this month.
Salon Technologies International Inc has 2 FDA actions in our database, including 2 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Salon Technologies International Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Salon Technologies International Inc have FDA actions?
Salon Technologies International Inc has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "D-0002-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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