Keystone Industries recalls Pearson Quality Topical Anesthetic Gel (20% Benzocaine) due to potential incomplete seals in containers. Affected units may leak or contaminate. Consumers should check product details and contact the manufacturer.
Defective container:may contain bottles with incomplete seals
Keystone Industries is recalling Pearson Quality Topical Anesthetic Gel (20% Benzocaine) because some containers may have incomplete seals. This could lead to leakage or contamination of the gel, posing a risk to users.
The gel's container may have incomplete seals, which could cause leakage or contamination. This might lead to the gel coming into contact with skin or other surfaces, potentially causing irritation or infection.
People who own or use Pearson Quality Topical Anesthetic Gel (20% Benzocaine) mint-flavored gel with a 1 oz (30 g) container. Dental professionals and patients using the product are most at risk.
Check for the product name 'Pearson Quality Topical Anesthetic Gel (20% Benzocaine)', mint flavor, 1 oz (30 g) container, and the expiration date of 04/01/2029. The product was manufactured for Pearson Dental Supply Inc. in Sylmar, CA.
Look for the product name, mint flavor, 1 oz (30 g) container, and expiration date of 04/01/2029 on the label.
The recall indicates a potential risk of incomplete seals, but the product is generally safe if the container is intact. Consumers should check for leaks or damage before use.
Check for the product name 'Pearson Quality Topical Anesthetic Gel (20% Benzocaine)', mint flavor, 1 oz (30 g) container, and expiration date of 04/01/2029.
The recall does not specify a remedy, so check the product details and contact Keystone Industries for further 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-0600-2026 — Keystone Industries Keystone Industries Hello, I own a Keystone Industries that is covered by recall D-0600-2026 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.
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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.
