Unrated Drug recall · FDA · Published February 2, 2026

Pro N: 5% Lidocaine Tattoo Numbing Spray Recall - Cgmp Deviations

Pro Numb recalls 5% lidocaine tattoo numbing spray due to cGMP deviations. Affected products include 1 fl oz and 4 oz bottles with specific lot numbers. Consumers should contact the manufacturer for details.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #D-0302-2026Drug Pro Numb ›

Recall notice

cGMP deviations

Take action

Contact the company

Recalling firmPro Numb Tattoo Numbing Spray LLC3778 Dixie Hwy Ne Ste C · Palm Bay, FL 32905-2727

✎ GovInfoNow plain-language explainer

Pro Numb is recalling its 5% lidocaine tattoo numbing spray because of manufacturing quality control issues. This recall affects specific bottle sizes and lot numbers, and consumers should check their product details to see if they are affected. Read more at govinfonow.com/recall/31494-pro-n-5-lidocaine-tattoo-numbing-spray-recall-cgmp-deviations.

Source Summary by GovInfoNow · govinfonow.com/recall/31494-pro-n-5-lidocaine-tattoo-numbing-spray-recall-cgmp-deviations · Updated August 17, 2026 · FDA enforcement record: FDA #D-0302-2026

Cite this page

“Pro N: 5% Lidocaine Tattoo Numbing Spray Recall - Cgmp Deviations.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/31494-pro-n-5-lidocaine-tattoo-numbing-spray-recall-cgmp-deviations. Based on FDA recall #D-0302-2026 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0302-2026%22&limit=1).

Pro Numb Tattoo Numbing Spray LLC recalled Pro Numb Tattoo Numbing Spray due to current Good Manufacturing Practice deviations, the Food and Drug Administration said on Feb. 2, 2026.

How to tell if you have it

Brand: Pro Numb
Product: Pro Numb Tattoo Numbing Spray, 5% Lidocaine
Sizes: 1 FL OZ/28.4 ML or 4 oz/120 mL per bottle
NDC: 83389-111-11
Lot Numbers: J01 through J14, J55 through J69
Distributed by: Pro Numb Tattoo numbing spray LLC
Distribution: Nationwide in the USA

The hazard

The recall involves current Good Manufacturing Practice deviations, according to the FDA.

Context

GovInfoNow's records show other recent recalls of similar products include Blossom Pharmaceuticals Globe Clotrimazole Cream Recall (2025-10-31), Wells Pharma Fentanyl Citrate Injectable Solution Recall (2026-04-01), and Baxter Healthcare Daptomycin Injection Recall (2026-08-06).

How to tell if you have this one

Check the product label for the brand 'Pro Numb', the size (1 fl oz or 4 oz), and the lot numbers J01 through J14 or J55 through J69. The product was distributed by Pro Numb Tattoo Numbing Spray LLC in Melbourne, Florida.

Brand
Pro Numb
Category
Drug

FDA recall event · 2 products

All 2 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

Classification
Class II
Status
Ongoing
Distribution
Nationwide in the USA

Recall number	Product, codes & lots	NDC
D-0302-2026	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; Lot Numbers J01 through J14, J55 through J69	83389-111-11
D-0303-2026	Pro Numb Tattoo Numbing Spray, For Sensitive Skin, 4% Lidocaine, [1FL OZ/28.4 ML or 4 oz/120 mL] per bottle, Distributed by: Pro Numb Tattoo numbing spray LLC, Melbourne, FL 32907, NDC 83389-112-11; Lot Number J15	83389-112-11

Based on the official FDA remedy

What to do — step by step

Check Product Details
Identify the lot number on the product label to determine if it is affected (J01 through J14 or J55 through J69).

Where it went and when

Where it was distributed

Distributed nationwide.

FDA distribution: “Nationwide in the USA” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA published this recall 16 days after the firm started it.

Feb 2, 2026Firm started the recall
Feb 9, 2026FDA classified it Class II
Feb 18, 2026Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

Similar recalls

Latest drug recalls

Keep exploring

Link to this recall

<a href="https://govinfonow.com/recall/31494-pro-n-5-lidocaine-tattoo-numbing-spray-recall-cgmp-deviations">Pro N: 5% Lidocaine Tattoo Numbing Spray Recall - Cgmp Deviations (GovInfoNow)</a>

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-0302-2026 (February 2, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0302-2026 to see it in context.
Plain-language summary written by qwen3:4b on August 17, 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.