HIGHFDA DRUG

Pro Numb Tattoo Numbing Spray Recalled Due to cGMP Violations

Pro Numb Tattoo Numbing Spray was recalled on February 2, 2026 due to cGMP deviations. The product, containing 4% lidocaine, is distributed by Pro Numb Tattoo Numbing Spray LLC. Consumers should stop using it immediately and contact the company for further guidance.

Official notice

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA DRUG
Recall date
February 2, 2026
Status
ACTIVE
Severity
8/10

Quick Facts at a Glance

Recall Date
February 2, 2026
Hazard Level
HIGH
Brands
PRO NUMB SENSITIVE SKIN, Pro Numb Tattoo Numbing Spray LLC
Category
Health & Personal Care
Sold At
Multiple Retailers
Geographic Scope
1 states
At-Risk Groups
GENERAL

What to Do Now

Use this page like a recall checklist: verify the product first, then act on the official remedy.

Immediate steps

  1. 1Stop using the product until you confirm whether it is included in the recall.
  2. 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
  3. 3Follow the official remedy from FDA - Drug Safety; save photos, receipts, labels, and correspondence before contacting the company.
  4. 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.

Check these identifiers

Brand
PRO NUMB SENSITIVE SKIN, Pro Numb Tattoo Numbing Spray LLC
Product type
Numbing Spray
Model numbers
Lot Number J15
UPC codes
83389-112, 83389-112-11
Sold at
Multiple Retailers
Where affected
ALL

Recall Timeline

Key dates and source checks for this recall record.

  1. Recall announced

    February 2, 2026

  2. Reported by FDA DRUG

    February 18, 2026

  3. RecallRadar source check

    February 25, 2026

  4. Consumer action

    Use the official remedy and keep documentation.

Hazard Information

cGMP deviations

What You Should Do

Consumers and healthcare providers should stop using this product immediately. Contact Pro Numb Tattoo Numbing Spray LLC or your healthcare provider for guidance. Notification method: Letter

About This Product

Pro Numb Tattoo Numbing Spray is designed to minimize pain during tattoo application, particularly for sensitive skin. Consumers often purchase it to ease discomfort associated with tattoo procedures.

Why This Is Dangerous

The cGMP deviations indicate that the product may not have been manufactured according to safety standards, potentially leading to ineffective or harmful effects.

Industry Context

This recall is not part of a broader industry pattern.

Real-World Impact

Consumers are advised to stop using the product immediately. There is a potential risk for adverse effects, and users may need to seek alternatives for pain management.

Practical Guidance

How to identify if yours is affected

  1. Check the product label for Lot Number J15.
  2. Confirm the NDC number 83389-112-11 to verify if your product is affected.
  3. Look for the distribution date range between January 1, 2026, and February 1, 2026.

Where to find product info

The Lot Number and NDC number can typically be found on the product packaging or label.

What timeline to expect

Expect 4-6 weeks for refund processing after contacting the manufacturer.

If the manufacturer is unresponsive

  • Document your correspondence with the company.
  • Reach out to consumer protection agencies for assistance.
  • Consider filing a complaint with the FDA.

How to prevent similar issues

  • Always check for recalls on health products before purchase.
  • Look for products with clear labeling about manufacturing practices.
  • Consult healthcare providers for trusted product recommendations.

Documentation advice

Keep receipts, correspondence with the manufacturer, and any medical records related to the use of the product.

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Product Details

The recalled product is Pro Numb Tattoo Numbing Spray, available in two sizes: 1 FL OZ (28.4 ML) and 4 oz (120 mL). It is distributed by Pro Numb Tattoo Numbing Spray LLC, based in Melbourne, Florida. The NDC number is 83389-112-11.

Key Facts

  • Recall date: February 2, 2026
  • Report date: February 18, 2026
  • Distribution: Nationwide in the USA
  • Hazard level: High

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: What to Do When You Find a Recalled Product

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Safety Assessment

Risk LevelHIGH
Severity Score
8/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Classification

Product TypeNumbing Spray
Sold At
Multiple Retailers

Product Details

Model Numbers
Lot Number J15
UPC Codes
83389-112
83389-112-11
Affected States
ALL
Report Date
February 18, 2026
Source Agency
FDA - Drug Safety
Recall Status
ACTIVE

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