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

Recalled July 5, 2023 · FDA recall Z-2044-2023 · Appliedvr

Hazard

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

Units

1 unit

Sold at

US: NY OUS: None

Description

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

Product

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

Manufacturer(s)

Appliedvr

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →