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Class II · ModerateActive recall

Pro Numb

Could cause temporary or reversible harm; serious harm is unlikely.

Does this affect you?
Check your lot numberLot Numbers J01 through J14, J55 through J69
Where it was soldNationwide in the USA
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.

What happened

cGMP deviations

What to do

  1. Check the lot number and expiry on your medicine against the recall above.
  2. Talk to your pharmacist or doctor before changing anything — don't stop on your own.
  3. Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).

Who makes it

Made byPro Numb Tattoo Numbing Spray LLC
Brand namePRO NUMB
Generic nameTATTOO NUMBING SPRAY
Active ingredient(s)EPINEPHRINE HYDROCHLORIDE, LIDOCAINE HYDROCHLORIDE
Distributed by / forPro Numb Tattoo numbing spray LLC, Melbourne, FL 32907
NDC83389-111-11
Show the full FDA record
Full product labelPro 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
Recalling firmPro Numb Tattoo Numbing Spray LLC
DistributionNationwide in the USA
QuantityN/A
Recall initiated2026-02-02
Report date2026-02-18
Recall completed—
Recall numberD-0302-2026
ClassificationClass II
FDA statusOngoing
Origin on filePalm Bay FL United States

Related

Recent drug recallsCheck another medication

Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗

This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.