Keystone Industries recalls Quala Dental Products topical anesthetic gel due to potential incomplete seals in containers. Affected units contain 20% benzocaine strawberry flavor gel, 1 oz (30g), made in USA. Consumers should check for incomplete seals and contact for remedy.
Defective container:may contain bottles with incomplete seals
Keystone Industries is recalling Quala Dental Products' topical anesthetic gel because some containers may have incomplete seals. This could allow the gel to leak or contaminate, posing a risk of accidental ingestion or skin irritation.
The gel's container may have incomplete seals, which could lead to leakage or contamination. This might cause accidental ingestion or skin irritation, especially in individuals with sensitive skin or children.
People who own or use Quala Dental Products' 20% benzocaine topical anesthetic gel (strawberry flavor, 1 oz) made in the USA are affected. Those with sensitive skin or children are at slightly higher risk due to potential skin irritation.
Check for the product name 'Quala Dental Products, Topical Anesthetic Gel, 20% Benzocaine, Strawberry Flavor' with net contents of 1 oz (30g). The product was made in the USA and has the NDC number 43128-034-30.
Inspect the container for incomplete seals, which may allow leakage or contamination.
The recall indicates potential incomplete seals, which could lead to leakage or contamination. If you have the product, check the seal first.
Look for the product name 'Quala Dental Products, Topical Anesthetic Gel, 20% Benzocaine, Strawberry Flavor' with net contents of 1 oz (30g). The product was made in the USA and has the NDC number 43128-034-30.
Check the container for incomplete seals. If you find an incomplete seal, stop using it and contact Keystone Industries for further instructions.
We’ve drafted a message you can send Keystone Industries to request your refund or repair — edit it as you like.
Subject: Recall D-0601-2026 — Keystone Industries Keystone Industries Hello, I own a Keystone Industries that is covered by recall D-0601-2026 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.
