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.
The product contains a non-functional component not referenced in product labeling.
Stimwave is recalling specific models of their StimQ Peripheral Nerve Stimulator Systems (PNS) because they contain a non-functional component that isn't listed in the product labeling. This issue doesn't cause immediate harm but means the device might not work as intended for pain relief.
The product contains a non-functional component that isn't referenced in the product labeling. This means the device might not work as intended for pain relief, but it doesn't cause immediate injury or health risks.
Users of the StimQ PNS Model 1. STQ4-RCV-A0 US and EU units with the serial numbers listed in the recall notice are affected. People using these devices for chronic pain management are most at risk of the device not functioning properly.
Check if your StimQ PNS Model 1. STQ4-RCV-A0 US or EU unit has a serial number listed in the provided list of numbers. The recall covers specific serial numbers across both US and EU versions.
Verify if your device's serial number appears in the list of affected serial numbers provided in the recall notice.
No, the device doesn't cause immediate injury or health risks. It contains a non-functional component not referenced in labeling, which means it might not work as intended for pain relief.
Yes, check if your device's serial number is in the list provided in the recall notice. If it is, contact Stimwave for further instructions.
The serial number is typically found on the device itself or in the packaging. Check the list of affected serial numbers in the recall notice to see if your device is included.
We’ve drafted a message you can send Stimwave to request your refund or repair — edit it as you like.
Subject: Recall Z-2928-2020 — Stimwave Stimwave Hello, I own a Stimwave that is covered by recall Z-2928-2020 from Stimwave. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
