Ecometics recalls menthol and camphor products due to CGMP manufacturing deviations. Products may not meet safety standards. Check UPCs and expiration dates for affected items.
CGMP Deviations: Products not manufactured under current good manufacturing practices.
Ecometics is recalling menthol and camphor products that were not made under current good manufacturing practices. This could mean the products don't meet safety standards, but the recall doesn't specify a risk of injury or illness.
The products were not manufactured under current good manufacturing practices, which means they may not meet safety standards. This could lead to issues with product quality or safety, but the recall does not specify a risk of injury or illness.
Owners of Ecometics ALCOLADO RELAMPAGO products with the listed UPCs and expiration dates are affected. People using these products for medicinal purposes may be at risk if the products don't meet safety standards.
Check for products with UPC 7 18864 20102 9 (7 fl oz) or UPC 7 18864 20110 4 (16 fl oz). Products with expiration dates listed as 10/23, 11/23, 3/24, or 5/24 are affected.
Look for the listed UPC codes and expiration dates to confirm if your product is affected.
The products were not manufactured under current good manufacturing practices, which means they may not meet safety standards.
Check the UPC codes and expiration dates listed in the recall to see if your product is affected. If it is, contact the manufacturer for further instructions.
The recall does not specify a risk of injury or illness, so there is no known danger to users.
We’ve drafted a message you can send Ecometics to request your refund or repair — edit it as you like.
Subject: Recall D-1098-2023 — Ecometics Ecometics Hello, I own a Ecometics that is covered by recall D-1098-2023 from Ecometics. 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.
