Why it was recalled
cGMP deviations
Product description
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, UPCs & expiration codes
Lot Numbers J01 through J14, J55 through J69
Where it was sold
Nationwide in the USA
What to do if you have this product
- Compare the lot number and expiration date on your package with the codes above.
- Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
- If you have symptoms you think are related, contact your doctor. In an emergency call 911.
- Report side effects to FDA MedWatch at 1-800-FDA-1088.
Recall details
- Recall number
- D-0302-2026
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- Feb 2, 2026
- FDA report date
- Feb 18, 2026
- Quantity
- N/A
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- Pro Numb Tattoo Numbing Spray LLC
Original FDA data
Every field from FDA enforcement report D-0302-2026, exactly as published.
Show all FDA fields
- City
- Palm Bay
- State
- FL
- Status
- Ongoing
- Country
- United States
- Event ID
- 98361
- Address
- 3778 Dixie Hwy Ne Ste C
- Code information
- Lot Numbers J01 through J14, J55 through J69
- Postal code
- 32905-2727
- Report date
- Feb 18, 2026
- Product type
- Drugs
- Recall number
- D-0302-2026
- Classification
- Class II
- Recalling firm
- Pro Numb Tattoo Numbing Spray LLC
- Reason for recall
- cGMP deviations
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- 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
- Distribution pattern
- Nationwide in the USA
- Recall initiation date
- Feb 2, 2026
- Initial firm notification
- Letter
- Center classification date
- Feb 9, 2026