FDA recall, , Moderate risk
Pro Numb Tattoo Numbing Spray
Pro Numb Tattoo Numbing Spray is recalling its Pro Numb Tattoo Numbing Spray because of cGMP deviations.
Summary by Recall Canary from the FDA notice
What happened
Pro Numb Tattoo Numbing Spray LLC, of Palm Bay, Florida, began recalling its Pro Numb Tattoo Numbing Spray on February 2, 2026, because of cGMP deviations. The recall covers the 5% Lidocaine and 4% Lidocaine versions, distributed nationwide in the USA. The FDA added the recall to its Enforcement Report on February 9, 2026, and it was in the weekly enforcement report on February 18, 2026.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medicine recalls:
- Check the FDA or company notice for instructions specific to this product.
- Ask your pharmacist or doctor whether your lot is affected and what to do.
Is your bottle affected?
2 products
Match the lot code and NDC listed under your product.
An NDC (National Drug Code) is usually printed on the drug's label.
Pro Numb Tattoo Numbing Spray, 5% Lidocaine, [1 fl oz/28.4 ml or 4 oz/120 mL] per bottle
- NDC
- 83389-111-11
- Lot code
- J01
- J14
- J55
- J69
Pro Numb Tattoo Numbing Spray, For Sensitive Skin, 4% Lidocaine, [1FL oz/28.4 ml or 4 oz/120 mL] per bottle
- NDC
- 83389-112-11
- Lot code
- J15
Recall details
- Company began the recall
- Sold in
Nationwide in the USA
- Company
- Pro Numb Tattoo Numbing Spray LLCPalm Bay, Florida
- Hazard
- Manufacturing problem
- Risk
Moderate risk
Taking it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- Event ID
- 98361
- Recall numbers
- D-0302-2026 to D-0303-2026
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
In FDA's weekly enforcement report
Listed on Recall Canary
Summary updated
