Keystone Industries recalls Dental City 20% Benzoic Acid Anesthetic Gel due to potential incomplete container seals. Consumers should check product details and contact Dental City for guidance.
Defective container:may contain bottles with incomplete seals
Keystone Industries is recalling Dental City TOPICAL ANESTHETIC GEL, BENZOCAINE 20%, Strawberry Flavor, 1 OZ (30 g) because the container may have incomplete seals. This could lead to the gel leaking or being exposed to contaminants, posing a risk of accidental ingestion or skin irritation.
The container may have incomplete seals, which could allow the gel to leak or become exposed to contaminants. This poses a risk of accidental ingestion or skin irritation, especially if the product is mishandled or used improperly.
Dental professionals and consumers who own or use the recalled Dental City topical anesthetic gel. Those with the product from the distribution date (3205 Yeager Dr., Green Bay, WI) are most at risk.
Check for the product name 'Dental City TOPICAL ANESTHETIC GEL, BENZOCAINE 20%, Strawberry Flavor, 1 OZ (30 g)' with NDC 69483-001-30 and expiration date 04/15/2029. The product was distributed by Dental City from 3205 Yeager Dr., Green Bay, WI.
Verify the product name, NDC 69483-001-30, and expiration date 04/15/2029 to confirm if it is recalled.
The recall indicates a potential risk of incomplete seals, which could lead to leakage or exposure. It is recommended to check for the specific product details and contact Dental City for further guidance.
The recall record does not specify a replacement option. Contact Dental City at 3205 Yeager Dr., Green Bay, WI for assistance.
The recall record does not provide specific instructions for disposal or return. Check the product details and contact Dental City for guidance.
We’ve drafted a message you can send Keystone Industries to request your refund or repair — edit it as you like.
Subject: Recall D-0604-2026 — Keystone Industries Keystone Industries Hello, I own a Keystone Industries that is covered by recall D-0604-2026 from Keystone Industries. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
