Quick Facts at a Glance
- Recall Date
- February 2, 2026
- Hazard Level
- HIGH
- Brands
- PRO NUMB, 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
- 1Stop using the product until you confirm whether it is included in the recall.
- 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
- 3Follow the official remedy from FDA - Drug Safety; save photos, receipts, labels, and correspondence before contacting the company.
- 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.
Check these identifiers
- Brand
- PRO NUMB, Pro Numb Tattoo Numbing Spray LLC
- Product type
- Tattoo Numbing Spray
- Model numbers
- Lot Numbers J01 through J14, J55 through J69
- UPC codes
- 83389-111, 83389-111-11
- Sold at
- Multiple Retailers
- Where affected
- ALL
Recall Timeline
Key dates and source checks for this recall record.
Recall announced
February 2, 2026
Reported by FDA DRUG
February 18, 2026
RecallRadar source check
February 25, 2026
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 a topical anesthetic designed to reduce pain during tattoo application. Consumers typically use this spray to alleviate discomfort associated with getting tattoos.
Why This Is Dangerous
The hazard arises from deviations in manufacturing practices, which can lead to compromised safety and effectiveness of the numbing spray. Such deviations may cause unexpected side effects or insufficient numbing.
Industry Context
This recall is not part of a broader industry pattern.
Real-World Impact
Consumers face potential risks if they continue to use the recalled product, as it may not provide the expected pain relief or could cause adverse reactions.
Practical Guidance
How to identify if yours is affected
- Check the product label for lot numbers J01 through J14 and J55 through J69.
- Confirm the product size, either 1 FL OZ or 4 oz, matches the recalled specifications.
- Look for the NDC number 83389-111-11 on the packaging.
Where to find product info
Lot numbers can typically be found on the bottom of the bottle or the packaging label.
What timeline to expect
Expect a timeline of 4-6 weeks for receiving a refund or replacement after submission of your request.
If the manufacturer is unresponsive
- Follow up with Pro Numb Tattoo Numbing Spray LLC via phone or email.
- Consider filing a complaint with the FDA if the company does not respond.
How to prevent similar issues
- When purchasing numbing sprays, look for products with clear labeling and compliance with cGMP standards.
- Check for user reviews and safety certifications before purchasing.
- Consult with professionals for recommendations on safe numbing agents.
Documentation advice
Keep receipts, product packaging, and any correspondence with the company as documentation for your records.
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Product Details
The recalled product is Pro Numb Tattoo Numbing Spray, containing 5% Lidocaine, available in 1 FL OZ and 4 oz sizes. It was distributed by Pro Numb Tattoo Numbing Spray LLC based in Melbourne, FL. The recall was initiated on February 2, 2026.
Key Facts
- Recalled product: Pro Numb Tattoo Numbing Spray
- Immediate stop-use recommended
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Safety Guide
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