Every recall we track for Stimwave Technologies Inc — 6 in all — plus the complaints and injury reports the public filed about them.
Stimwave recalls 200+ units of StimQ Peripheral Nerve Stimulator System (PNS) Model STQ4-SPR-BO US due to a non-functional component not referenced in product labeling. This may cause improper therapy delivery. Affected units have specific serial numbers listed in the recall notice.
Stimwave recalls StimQ Peripheral Nerve Stimulator Systems with specific serial numbers due to a non-functional component not referenced in product labeling.
Stimwave recalls StimQ PNS Model 1. STQ4-RCV-A0 US and EU units with non-functional components not referenced in product labeling. Affected units have serial numbers listed in the recall notice.
Stimwave recalls two models of StimQ PNS devices due to a non-functional component not listed in labeling. Affected units include specific US and EU serial numbers for chronic pain therapy devices.
Stimwave recalls StimQ Peripheral Nerve Stimulator System Model FR4A-TRL-AO US due to a non-functional component not referenced in product labeling. Affected units include specific serial numbers listed in the recall. No remedy is provided in the official notice.
Stimwave recalls StimQ PNS Models FR4A-SPR-BO US due to a non-functional component not listed in product labeling. Affected units have specific serial numbers.
