Keystone Industries recalls Safco SensiCaine-Ultra topical anesthetic gel due to potential incomplete container seals. This may lead to product leakage or contamination. Consumers should check for the specific model and NDC number.
Defective container:may contain bottles with incomplete seals
Keystone Industries is recalling Safco SensiCaine-Ultra topical anesthetic gel because some containers may have incomplete seals. This could cause the gel to leak or become contaminated, posing a risk of accidental ingestion or skin irritation.
The gel's container may have incomplete seals, which could allow the product to leak or become contaminated. This might lead to accidental ingestion or skin irritation if the gel comes into contact with the skin without proper protection.
People who own or use Safco SensiCaine-Ultra topical anesthetic gel with the specific NDC number 67239-0223-1. Those most at risk are individuals who apply the gel to their skin without proper containment.
Check for the product name 'Safco SensiCaine-Ultra (20% Benzocaine)', strawberry flavor, 1 oz. (29.6mL) container. The NDC number is 67239-0223-1 and it was distributed by Safco Dental Supply Co. in the USA.
Inspect the container for incomplete seals, which may allow leakage or contamination.
The recall indicates a potential risk of incomplete seals, but the product is generally safe if the container is properly sealed. Consumers should check for incomplete seals before use.
Look for the product name 'Safco SensiCaine-Ultra (20% Benzocaine)', strawberry flavor, 1 oz. (29.6mL) container with NDC number 67239-0223-1.
Inspect the container for incomplete seals. If found, stop using it and contact the manufacturer 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-0606-2026 — Keystone Industries Keystone Industries Hello, I own a Keystone Industries that is covered by recall D-0606-2026 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.
