HTO Nevada Blue Gel Anesthetic Recall: Discoloration Risk

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Recalling firmHTO Nevada, Inc.6400 Rosewood St, N/A · Lake Oswego, OR 97035-5392

No email on file — use the official page, write to the address above instead.

✎ GovInfoNow plain-language explainer

What happened, in plain English

HTO Nevada is recalling 1-ounce blue gel anesthetic products because the epinephrine ingredient may have discoloration. This could affect the safety and effectiveness of the product for medical procedures.

Why it’s dangerous

The epinephrine ingredient in the anesthetic may have discoloration due to a raw material issue. This could potentially affect the product's safety and effectiveness, though the risk is low for proper use.

Who’s affected

Licensed medical professionals who use this anesthetic for pain-sensitive procedures. The risk is lowest for users who follow proper handling procedures.

How to tell if you have this one

Check for the 1-ounce blue gel anesthetic with NDC code 80069-008-01. Products were distributed by Dermal Source in Portland, OR with lot numbers 796CP-0006 (expiring 02/2024) and 796CP-0007 (expiring 03/2024).

Brand
HTO Nevada
Category
Drug

Based on the official FDA remedy

What to do — step by step

Check Product Details
Verify the NDC code 80069-008-01 and lot numbers 796CP-0006 or 796CP-0007 on the product label.

✎ GovInfoNow

Questions people ask

Is this product safe to use?

The recall is due to potential discoloration in the epinephrine ingredient, but the product is still safe for use by licensed professionals following standard procedures.

How can I check if I have the recalled product?

Look for the NDC code 80069-008-01 and lot numbers 796CP-0006 (expiring 02/2024) or 796CP-0007 (expiring 03/2024) on the product label.

What should I do if I have the recalled product?

The recall does not require immediate action; check the product details and contact Dermal Source at 1-888-568-3223 if you have concerns.

Take action

Contact HTO Nevada

We’ve drafted a message you can send HTO Nevada to request your refund or repair — edit it as you like.

✉️ Open in emailCompany site

Subject: Recall D-0270-2023 — HTO Nevada HTO Nevada

Hello,

I own a HTO Nevada that is covered by recall D-0270-2023 from HTO Nevada.

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-0270-2023 (February 9, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0270-2023 to see it in context.
Plain-language summary written by qwen3:4b on August 18, 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.

HTO Nevada, Inc. recalls New & Improved Blue Gel Anesthetic, to reduce pain and swelling during pain sensitive procedures, 1 oz bottle,

Lower-risk recall