RecallRadar
ModerateReported February 18, 2026

Pro Numb Tattoo Numbing Spray, 5% Lidocaine

Recalled by Pro Numb Tattoo Numbing Spray LLC

Product image for Pro Numb Tattoo Numbing Spray, 5% Lidocaine, [1 FL OZ/28.4 ML or 4 oz/120 mL] per bottle, Distributed by: Pro Numb Tattoo numbing spray LLC, Melbourne, FL 32907, NDC 83389-111-11
Product image via DailyMed (National Library of Medicine). It may show general packaging and not the exact recalled lot — always confirm using the codes below.

Class II — moderate

Using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.

Pro Numb Tattoo Numbing Spray LLC has recalled Pro Numb Tattoo Numbing Spray, 5% Lidocaine, according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on February 18, 2026 and was initiated on February 2, 2026. It is classified as a Class II recall, which means using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.

Below is a plain-English summary of what was recalled, why it was recalled, how to tell whether you have the affected product, and what steps you can take. For the complete and most current details, you can view the FDA record linked further down this page.

What was recalled?

This recall covers Pro Numb Tattoo Numbing Spray, 5% Lidocaine, with approximately N/A affected. The company behind the recall is Pro Numb Tattoo Numbing Spray LLC, based in Palm Bay, FL. The FDA describes the product as: “Pro Numb Tattoo Numbing Spray, 5% Lidocaine, [1 FL OZ/28.4 ML or 4 oz/120 mL] per bottle, Distributed by: Pro Numb Tattoo numbing spray LLC, Melbourne, FL 32907, NDC 83389-111-11”

Why was Pro Numb Tattoo Numbing Spray, 5% Lidocaine recalled?

According to the FDA, the stated reason for the recall is: “cGMP deviations.” In plain terms, this recall relates to a manufacturing quality issue (CGMP).

CGMP stands for Current Good Manufacturing Practice — the FDA's quality rules for how medicines must be made, tested, and documented. A CGMP-related recall means the manufacturing process did not meet those standards. It does not automatically mean the medicine is harmful, but the FDA cannot be confident in its quality, so it is removed from the market.

What should you do?

If you think you may have bought Pro Numb Tattoo Numbing Spray, 5% Lidocaine, compare it against the product description and identifying codes (Lot Numbers J01 through J14, J55 through J69) before using it. This recall is currently listed as ongoing.

The general guidance for a matching product is to stop using it and follow the instructions in the official FDA recall notice, which may include a repair, replacement, refund, or safe disposal. When in doubt, contact Pro Numb Tattoo Numbing Spray LLC or your local health authority.

About this recall

This recall was distributed in FL. RecallRadar summarizes recall information from public FDA data to make it easier to understand. We are an independent service and are not affiliated with the FDA or any government agency, so please always refer to the official source for the authoritative record — and note the “last synced” date shown on this page, since recall details can change over time.

Full recall details

Status
Ongoing
Date reported
February 18, 2026
Recall started
February 2, 2026
Distributed in
FL
What was recalled
Pro Numb Tattoo Numbing Spray, 5% Lidocaine, [1 FL OZ/28.4 ML or 4 oz/120 mL] per bottle, Distributed by: Pro Numb Tattoo numbing spray LLC, Melbourne, FL 32907, NDC 83389-111-11
Why it was recalled (as stated by the FDA)
cGMP deviations
How to identify the affected product
Lot Numbers J01 through J14, J55 through J69
Amount recalled
N/A

What you can do

Check whether any product you have matches the description and codes above. If it does, stop using it and follow the instructions in the official recall notice. When in doubt, contact the company or your local health authority.

Quick answers

Why was Pro Numb Tattoo Numbing Spray, 5% Lidocaine recalled?+

According to the FDA: cGMP deviations

How serious is this recall?+

Class II — moderate. Using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.

What should I do if I have Pro Numb Tattoo Numbing Spray, 5% Lidocaine?+

Compare your product against the description and identifying codes on this page. If it matches, stop using it and follow the instructions in the official recall notice — this usually means returning it for a refund or discarding it. When in doubt, contact the company or your local health authority.

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View the official FDA record

Opens the U.S. Food and Drug Administration (FDA) data for this recall.

Recall number: D-0302-2026. Information last synced from the FDA on July 5, 2026.

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