Pro Numb Tattoo Numbing Spray, For Sensitive Skin, 4% Lidocaine, [1FL OZ/28.4 ML or 4 oz/120 mL] per bottle, Distributed
Summary
The FDA issued a Class II for Pro Numb Tattoo Numbing Spray, For Sensitive Skin, 4% Lidocaine, [1FL OZ/28.4 ML by Pro Numb Tattoo Numbing Spray LLC. Reason: cGMP deviations.
Details
Source
Drug Recall
External ID
D-0303-2026
Action Date
2026-02-18
Status
Ongoing
Category
drug
Product Description
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/Code Info: Lot Number J15
Quantity Affected: N/A
Reason for Recall
cGMP deviations
Distribution
Nationwide in the USA
Type: Voluntary: Firm initiated
Recall Initiated: 2026-02-02
Company
Palm Bay, FL
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 73 drug recalls issued in the same week, part of 267 drug-related FDA actions this month.
Pro Numb Tattoo Numbing Spray LLC has 2 FDA actions in our database, including 2 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Pro Numb Tattoo Numbing Spray LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Pro Numb Tattoo Numbing Spray LLC have FDA actions?
Pro Numb Tattoo Numbing Spray LLC has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "D-0303-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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