Webrx dba RxPalace.com recalls BonaDur For Men (lidocaine) spray, 10 mg per spray, Net Contents .25 fl. oz. (7.4 mL) spray bottles, Manufactured by
RxPalace recalls BonaDur For Men lidocaine spray due to manufacturing deviations. Products may not meet current good manufacturing practices standards.
Recall notice
CGMP Deviations: not manufactured according to current good manufacturing practices.
Contact the company & request your remedy
What happened, in plain English
RxPalace is recalling BonaDur For Men lidocaine spray bottles that were manufactured without following current good manufacturing practices. This recall is due to potential quality issues with the product. Read more at govinfonow.com/recall/40885-rxpalace-bonadur-for-men-lidocaine-spray-recall-cgmp-manufacturing-deviations.
Source Summary by GovInfoNow · govinfonow.com/recall/40885-rxpalace-bonadur-for-men-lidocaine-spray-recall-cgmp-manufacturing-deviations · Updated October 7, 2026 · FDA enforcement record: FDA #D-0421-2018
Cite this page
“RxPalace BonaDur For Men Lidocaine Spray Recall: CGMP Manufacturing Deviations.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/40885-rxpalace-bonadur-for-men-lidocaine-spray-recall-cgmp-manufacturing-deviations. Based on FDA recall #D-0421-2018 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0421-2018%22&limit=1).
Why it’s dangerous
The product was manufactured without following current good manufacturing practices, which could lead to quality issues. This may affect the safety and effectiveness of the lidocaine spray.
Who’s affected
People who own or use BonaDur For Men lidocaine spray bottles with the specific lot number and expiration date listed in the recall notice are affected. Those using the product for medical purposes may be at risk if the product does not meet quality standards.
How to tell if you have this one
Check for the product name 'BonaDur For Men', 10 mg per spray, 0.25 fl. oz. (7.4 mL) size, manufactured by WebRx Pharmacy Palace in Sarasota, FL. Look for the lot number 17JXIII and expiration date 12/31/2019 on the label.
- Brand
RxPalace- Category
Drug
What to do — step by step
Check Product Label
Look for the lot number 17JXIII and expiration date 12/31/2019 on the BonaDur For Men lidocaine spray bottle.
Questions people ask
Is this product safe to use?
The recall states the product was manufactured without following current good manufacturing practices, but does not specify if it is safe to use. The official notice does not provide details on safety.
What should I do if I have this product?
The recall does not specify any remedy or action steps for affected products. The official notice does not provide instructions on what to do with the product.
How can I confirm if my product is recalled?
Check the product label for the lot number 17JXIII and expiration date 12/31/2019. The official notice does not provide additional identification methods.
Contact RxPalace
We’ve drafted a message you can send RxPalace to request your refund or repair — edit it as you like.
Subject: Recall D-0421-2018 — RxPalace RxPalace Hello, I own a RxPalace that is covered by recall D-0421-2018 from RxPalace. 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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Where this comes from
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.
- Official source: FDA Recall #D-0421-2018 (February 7, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0421-2018 to see it in context.
- Plain-language summary written by qwen3:4b on October 7, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.