HIGH

Pro Numb Tattoo Numbing Spray Recalled Due to cGMP Deviations

Pro Numb Tattoo Numbing Spray was recalled due to cGMP deviations. The recall affects products distributed nationwide in the USA. Consumers should stop using the spray immediately and contact Pro Numb Tattoo Numbing Spray LLC for guidance.

Quick Facts at a Glance

Recall Date
February 2, 2026
Hazard Level
HIGH
Brand
PRO NUMB
Category
Health & Personal Care
Sold At
Multiple Retailers
Geographic Scope
1 states
At-Risk Groups
GENERAL

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

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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.

The Hazard

The recall stems from deviations from current Good Manufacturing Practices (cGMP). These deviations can lead to compromised product quality and safety.

Reported Incidents

No specific incidents, injuries, or deaths have been reported related to this recall. However, the potential for adverse effects exists due to the manufacturing deviations.

What to Do

Consumers should immediately discontinue use of the product. For guidance, contact Pro Numb Tattoo Numbing Spray LLC or consult your healthcare provider.

Contact Information

For more information, consumers can visit the recall notice at the FDA website or contact Pro Numb Tattoo Numbing Spray LLC directly.

Key Facts

  • Recalled product: Pro Numb Tattoo Numbing Spray
  • Contains 5% Lidocaine
  • Distributed nationwide
  • Immediate stop-use recommended

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Safety Assessment

Risk LevelHIGH
Severity Score
8/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Classification

Product TypeTattoo Numbing Spray
Sold At
Multiple Retailers

Product Details

Model Numbers
Lot Numbers J01 through J14
J55 through J69
UPC Codes
83389-111
83389-111-11
Affected States
ALL
Report Date
February 18, 2026
Source Agency
FDA - Drug Safety
Recall Status
ACTIVE

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