The Recall Desk
ModerateFDA (Drugs)·D-0303-2026·Announced 2026-02-18

Pro Numb tattoo numbing spray recalled for manufacturing standard violations

Pro Numb Tattoo Numbing Spray (lot J15) is recalled nationwide due to manufacturing process deviations. The voluntary recall was initiated February 2, 2026.

What this means for you

Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.

Our severity reasoning: This is a FDA Class II recall with no reported illnesses or injuries, initiated voluntarily by the manufacturer for manufacturing process deviations. The hazard is theoretical rather than confirmed.

Plain-English summary

Pro Numb Tattoo Numbing Spray for Sensitive Skin, containing 4% Lidocaine, in 1 FL OZ or 4 OZ bottles (Lot Number J15), is being recalled nationwide. The product is manufactured by Pro Numb Tattoo Numbing Spray LLC, located in Melbourne, Florida.

The manufacturer voluntarily initiated the recall due to deviations from current Good Manufacturing Practice (cGMP) standards in the manufacturing process. The FDA has classified this as a Class II recall.

Consumers who have purchased this product should stop using it. For more information or questions, consumers can contact the manufacturer or their healthcare provider.

The recalled product

Product
PRO NUMB SENSITIVE SKIN (NUMBING SPRAY)
Brand
PRO NUMB SENSITIVE SKIN
Manufacturer
Pro Numb Tattoo Numbing Spray LLC
Category
Drug — Topical Anesthetic
Hazard
  • manufacturing-defect

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (1)

  • Lot Number J15

Distribution

Distributed nationwide across the United States.

Related recalls

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