A single bottle of BonaDur For Men (lidocaine) spray, used for numbing or topical pain relief, has been recalled because it was not manufactured according to current good manufacturing practices. This specific 0.25 fl. oz. (7.4 mL) spray bottle was distributed in New York. Because of these manufacturing failures, the safety and quality of the product cannot be guaranteed.
Products not manufactured according to strict safety standards may be ineffective or contain incorrect levels of active ingredients, potentially leading to skin irritation or inadequate pain relief.
Healthcare consultation and refund
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.