Pro Numb Tattoo Numbing Spray with 4% lidocaine for sensitive skin is recalled due to cGMP deviations. Affected products include 1 fl oz and 4 oz bottles. Consumers should contact the manufacturer for details.
cGMP deviations
Pro Numb Tattoo Numbing Spray for sensitive skin with 4% lid: 1 fl oz and 4 oz bottles are recalled because of manufacturing quality issues. This could affect product safety and effectiveness.
The recall is due to cGMP deviations, which are manufacturing quality issues that could affect product safety and effectiveness. These deviations might lead to inconsistent product quality or potential safety risks, though the specific hazard isn't detailed in the recall notice.
People who purchased the Pro Numb Tattoo Numbing Spray for sensitive skin with 4% lidocaine in 1 fl oz or 4 oz bottles are affected. Those with sensitive skin may be at higher risk due to the product's intended use.
Check for the product name 'Pro Numb Tattoo Numbing Spray', 4% lidocaine, and bottle sizes of 1 fl oz or 4 oz. The lot number J15 and NDC 83389-112-11 are also associated with the recalled items.
Reach out to Pro Numb Tattoo Numbing Spray LLC for specific instructions on how to handle the recalled product.
The recall states there were cGMP deviations, but the official notice does not specify if the product is safe to use.
The recall does not provide a specific remedy, so contact the manufacturer for details.
Look for the product name 'Pro Numb Tattoo Numbing Spray', 4% lidocaine, and bottle sizes of 1 fl oz or 4 oz. The lot number J15 and NDC 83389-112-11 are also associated with the recalled items.
We’ve drafted a message you can send Pro Numb Tattoo to request your refund or repair — edit it as you like.
Subject: Recall D-0303-2026 — Pro Numb Tattoo Pro Numb Tattoo Hello, I own a Pro Numb Tattoo that is covered by recall D-0303-2026 from Pro Numb Tattoo. 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.
