Pro Numb Tattoo Numbing Spray LLC is recalling two types of lidocaine numbing sprays because of manufacturing deviations (cGMP deviations) that could impact product quality and safety. The recall includes Pro Numb Tattoo Numbing Spray (5% Lidocaine) and the version for Sensitive Skin (4% Lidocaine) sold in 1-ounce and 4-ounce bottles. Consumers who have these products should contact their healthcare provider if they experience any issues and return the product or throw it away.
Manufacturing deviations can lead to inconsistent drug potency or potential contamination, which may cause the product to be ineffective or lead to unexpected skin reactions or infections at the site of application.
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Distributed by: Pro Numb Tattoo numbing spray LLC, Melbourne, FL 32907.
Distributed by: Pro Numb Tattoo numbing spray LLC, Melbourne, FL 32907.
If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.
This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.
AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.
Sources: FDA iRES · Raw API Response
openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.