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Completed

RelieVR REF: RVX-2002, Rx Only. Virtual reality behavioral therapy device for pain relief.

FDA Recall Z-2044-2023 · Posted 2023-06-30

Recalling FirmAppliedvr
Recall StatusCompleted
Product CodeQRA
Date Initiated2023-02-27
Product Quantity1 unit

Reason for Recall

There is the potential for the program software to malfunction which will not allow it to move forward to the next session.

Firm Action

On May, 2, 2023, AppliedVR provided customers with a Medical Device Recall notification in person. The recall notification informed the customer that the device was being recalled. For questions contact AppliedVR or your Health Care Provider.

Root Cause

Software Manufacturing/Software Deployment

Distribution Pattern

US: NY OUS: None

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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