Appliedvr recalls RelieVR RVX-2: Rx Only VR therapy device for pain relief due to potential software malfunction preventing session progression. Affected units have specific serial numbers and UDI codes.
There is the potential for the program software to malfunction which will not allow it to move forward to the next session.
Appliedvr is recalling its RelieVR RVX-2002 virtual reality therapy device for pain relief because software issues might prevent it from moving to the next therapy session. This could disrupt treatment for users who rely on the device.
The software may malfunction and stop the device from advancing to the next therapy session. This could prevent users from completing their treatment plan, especially if they need consistent sessions for pain management.
Users with the RelieVR RVX-2002 device for pain relief therapy are affected. Those who use the device for medical treatment under a prescription are most at risk of interrupted therapy.
Check for the serial number PA7940RGG5130514B or UDI code 0100850038247027211001077 on the device. The device is only for prescription use (Rx Only).
Verify if the device is functioning properly by attempting to start a new session.
The device may have software issues that prevent it from moving to the next session, but it is not unsafe to use. Users should check if it functions correctly.
The recall does not specify a remedy, so users should check if the device functions properly and contact Appliedvr for assistance.
Look for the serial number PA7940RGG5130514B or UDI code 0100850038247027211001077 on the device. The device is only for prescription use (Rx Only).
We’ve drafted a message you can send Appliedvr to request your refund or repair — edit it as you like.
Subject: Recall Z-2044-2023 — Appliedvr Appliedvr Hello, I own a Appliedvr that is covered by recall Z-2044-2023 from Appliedvr. 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.
