FDA Recall D-0303-2026
Pro Numb Tattoo Numbing Spray LLC · Palm Bay, FL
Class II Ongoing 101 days on record
Moderate impact — Class II recall — temporary or medically reversible adverse health consequence possible; remote probability of serious adverse health consequence.
Product
Pro Numb Tattoo Numbing Spray, For Sensitive Skin, 4% Lidocaine, [1FL OZ/28.4 ML or 4 oz/120 mL] per bottle, Distributed by: Pro Numb Tattoo numbing spray LLC, Melbourne, FL 32907, NDC 83389-112-11
Reason for recall
cGMP deviations
Recall record
- Recall number
D-0303-2026- Classification
- Class II
- Status
- Ongoing
- Voluntary or mandated
- Voluntary: Firm initiated
- Firm notification
- Letter
- Distribution
- Nationwide in the USA
- Recall initiated
- 2026-02-02
- Classified by FDA Center
- 2026-02-09
- FDA published
- 2026-02-18
- Recalling firm
- Pro Numb Tattoo Numbing Spray LLC
- Firm location
- Palm Bay, FL
Drug identification
- Brand name(s)
- PRO NUMB SENSITIVE SKIN
- Generic name(s)
- NUMBING SPRAY
- Manufacturer(s)
- Pro Numb Tattoo Numbing Spray LLC
- NDC(s)
83389-112- Route(s)
- TOPICAL
Operational response
Class II recalls indicate possible temporary or reversible health consequences. Remove affected lots from active dispensing. Segregate inventory. Check the firm’s recall notification for guidance on patient outreach.
For the official FDA enforcement record, see FDA's Recall Search.