FDA recall record

Salon Technologies International Sanitizing Hand Spray 80% (alcohol 80% v/v) recall — FDA D-0001-2023

GMP Deviations: FDA analysis found product to contain acetaldehyde and acetal above specification limits.

Class IIclassification
D-0001-2023official record ID
Oct 12, 2022report date

Recall record at a glance

Official recordD-0001-2023
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmSalon Technologies International Inc.
Report dateOct 12, 2022
Recall initiation dateSep 14, 2022
Quantity1656 bottles
LocationOrlando, FL, United States

Official product description

Sanitizing Hand Spray 80% (alcohol 80% v/v) Packaged in 2 FL OZ (60 mL) bottles, Salon Technologies International 8810 Commodity Circle STE 22-23, Orlando, FL 32819, UPC 6 96952 12904 5

Why the product was recalled

GMP Deviations: FDA analysis found product to contain acetaldehyde and acetal above specification limits.

Distribution information

FL and WA only

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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