Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
StimQ Peripheral Nerve Stimulator System (PNS) Model 1. STQ4-RCV-A0 US Recalled by Stimwave Technologies Inc Due to The product contains a non-functional component not referenced...
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 Stimwave Technologies Inc directly.
Affected Products
StimQ Peripheral Nerve Stimulator System (PNS) Model 1. STQ4-RCV-A0 US and 2.STQ4-RCV-A0 EU - Product Usage: is used for peripheral neural stimulation to provide therapeutic relief for chronic, intractable pain of peripheral nerve origin. The therapy utilizes pulsed electrical current to create an electrical energy field that acts on peripheral nerves in the limbs and torso to alter the transmission of pain signals to the brain.
Quantity: 2444 units
Why Was This Recalled?
The product contains a non-functional component not referenced in product labeling.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Stimwave Technologies Inc
Stimwave Technologies Inc has 6 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report