Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Algostim LLC Recalled by QiG Group LLC Due to The implantable pulse generator (IPG) model 2408 had...
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 QiG Group LLC directly.
Affected Products
Algostim LLC, Algovita Implanted Pulse Generator stimulator, Model 2408 ( 3 x 8 channel)
Quantity: 40
Why Was This Recalled?
The implantable pulse generator (IPG) model 2408 had suboptimal performance establishing a connection to the external devices unless they were brought into close proximity (as close as 5 cm). The following functions may not be available: Reprogramming the stimulator, Adjusting stimulation parameters (on/off, intensity modifications, stimulation program selection), and Recharging the stimulator.
Where Was This Sold?
Distributed in Germany and Luxembourg.
About QiG Group LLC
QiG Group LLC 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