Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
GentleWave System Posterior CleanFlow Procedure Instrument with Matrices (Single) REF Recalled by Sonendo Inc Due to Procedure Instruments with erroneous unit carton labels.
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Sonendo Inc directly.
Affected Products
GentleWave System Posterior CleanFlow Procedure Instrument with Matrices (Single) REF GW-PST-PI01
Quantity: 16 instruments
Why Was This Recalled?
Procedure Instruments with erroneous unit carton labels.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Sonendo Inc
Sonendo Inc has 3 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report