Pro Numb recalls 5% lidocaine tattoo numbing spray due to cGMP deviations. Affected products include 1 fl oz and 4 oz bottles with specific lot numbers. Consumers should contact the manufacturer for details.
cGMP deviations
Pro Numb is recalling its 5% lidocaine tattoo numbing spray because of manufacturing quality control issues. This recall affects specific bottle sizes and lot numbers, and consumers should check their product details to see if they are affected.
The product was manufactured with cGMP (current good manufacturing practice) deviations, which means the quality control process did not meet industry standards. This could potentially lead to inconsistent product quality or safety issues, though the exact risk is not clearly defined in the recall notice.
Tattoo artists and consumers who own the recalled 5% lidocaine numbing spray bottles. Those with the specific lot numbers J01 through J14 or J55 through J69 are most at risk.
Check the product label for the brand 'Pro Numb', the size (1 fl oz or 4 oz), and the lot numbers J01 through J14 or J55 through J69. The product was distributed by Pro Numb Tattoo Numbing Spray LLC in Melbourne, Florida.
Identify the lot number on the product label to determine if it is affected (J01 through J14 or J55 through J69).
The recall notice states there were cGMP deviations, but it does not specify if the product is safe to use. Consumers should check the lot number and contact the manufacturer for more information.
The recall notice does not provide a specific remedy or action for affected products. Consumers should check the lot number and contact the manufacturer for further instructions.
Look for the lot numbers J01 through J14 or J55 through J69 on the product label. The product was distributed by Pro Numb Tattoo Numbing Spray LLC in Melbourne, Florida.
We’ve drafted a message you can send Pro Numb to request your refund or repair — edit it as you like.
Subject: Recall D-0302-2026 — Pro Numb Pro Numb Hello, I own a Pro Numb that is covered by recall D-0302-2026 from Pro Numb. 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.
