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.
The product contains a non-functional component not referenced in product labeling.
Stimwave is recalling 200+ units of their StimQ Peripheral Nerve Stimulator System (PNS) Model STQ4-SPR-BO US because it contains a non-functional component that isn't mentioned in the product labeling. This could lead to improper pain therapy delivery. The recall includes specific serial numbers listed in the notice.
The product contains a non-functional component that isn't referenced in the product labeling. This means the device may not deliver the intended pain therapy properly, but it doesn't cause immediate injury or malfunction.
Users of the StimQ Peripheral Nerve Stimulator System (PNS) Model STQ4-SPR-BO US for chronic pain therapy are affected. Most users are likely to be the ones who purchased the device for medical treatment.
Check if your StimQ Peripheral Nerve Stimulator System (PNS) has the Model STQ4-SPR-BO US with the specific serial numbers listed in the recall notice. The recall covers 200+ units with serial numbers starting with 211668 and other patterns.
Look for the serial number on your StimQ device. If it matches the list of affected serial numbers provided in the recall notice, it is part of this recall.
Check if your device's serial number is listed in the recall notice. The recall covers specific serial numbers starting with patterns like 211668 and 2B11767.
Check your device's serial number against the list provided in the recall notice. If it's affected, you don't need to take action as the hazard is low risk and doesn't cause immediate injury.
The recall covers 200+ units with specific serial numbers listed in the notice.
We’ve drafted a message you can send Stimwave to request your refund or repair — edit it as you like.
Subject: Recall Z-2932-2020 — Stimwave Stimwave Hello, I own a Stimwave that is covered by recall Z-2932-2020 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.
