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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Low RiskFDA Drug
Medications & Supplements/Topical Products

Webrx dba RxPalace.com: BonaDur For Men (Lidocaine) Spray Recalled for Manufacturing Deviations

Agency Publication Date: February 14, 2018
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Summary

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.

Risk

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.

What You Should Do

  1. Check your medication for BonaDur For Men (lidocaine) spray, 10 mg per spray, in a 0.25 fl. oz. (7.4 mL) bottle.
  2. Locate the lot number and expiration date on the packaging to see if they match Lot 17JXIII with an expiration date of 12/31/2019.
  3. If you have the affected product, stop using it immediately.
  4. Contact your healthcare provider or pharmacist for guidance regarding any health concerns or alternative treatments.
  5. Return any unused product to the place of purchase for a refund and contact WebRx Pharmacy Palace at 501 N Beneva Rd Ste 550, Sarasota, Florida for further instructions.
  6. For additional questions, call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA).

Your Remedy Options

💰Full Refund

Healthcare consultation and refund

How to: Contact your healthcare provider or pharmacist for guidance. Return any unused product to the pharmacy for a refund

Affected Products

Product: BonaDur For Men (lidocaine) spray (0.25 fl. oz. / 7.4 mL)
Model:
NDC 70582-999-74
Recall #: D-0421-2018
Lot Numbers:
17JXIII (Exp. 12/31/2019)
Date Ranges: Exp. 12/31/2019

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 79172
Status: Resolved
Manufacturer: Webrx dba RxPalace.com
Sold By: WebRx Pharmacy Palace
Manufactured In: United States
Units Affected: 1 bottle
Distributed To: New York

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.