FDA found acetaldehyde and acetal levels in Salon Technologies Sanitizing Hand Spray 80% exceed safety limits. Consumers should check product details and contact the manufacturer for recalls.
GMP Deviations: FDA analysis found product to contain acetaldehyde and acetal above specification limits.
Salon Technologies International is recalling its Sanitizing Hand Spray 80% (alcohol 80% v/v) due to FDA findings that it contains acetaldehyde and acetal above specified limits. This could pose a risk to health from chemical exposure.
The spray contains acetaldehyde and acetal levels higher than what the FDA allows. These chemicals can cause skin irritation or respiratory issues when exposed to high concentrations.
Anyone who owns or uses the recalled Sanitizing Hand Spray 80% (alcohol 80% v/v) in 2 FL OZ bottles with lot number 20-018. People with sensitive skin or respiratory issues may be at higher risk.
Check for the product name 'Sanitizing Hand Spray 80% (alcohol 80% v/v)' in 2 FL OZ (60 mL) bottles. Look for lot number 20-018 and expiration date 4/3/2023 on the label.
Look for the lot number 20-018 and expiration date 4/3/2023 on the bottle label.
The FDA found the product contains acetaldehyde and acetal above specified limits, which could cause skin irritation or respiratory issues. The manufacturer has not provided a remedy.
Check for the product name 'Sanitizing Hand Spray 80% (alcohol 80% v/v)' in 2 FL OZ (60 mL) bottles with lot number 20-018 and expiration date 4/3/2023.
The manufacturer has not provided a remedy, so contact Salon Technologies International for further instructions.
We’ve drafted a message you can send Salon Technologies International to request your refund or repair — edit it as you like.
Subject: Recall D-0001-2023 — Salon Technologies International Salon Technologies International Hello, I own a Salon Technologies International that is covered by recall D-0001-2023 from Salon Technologies International. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
