Appliedvr: Medical Device Recall in 2023 - (Recall #: Z-2044-2023)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: February 27, 2023

Date Posted: July 5, 2023

Recall Number: Z-2044-2023

Event ID: 92389

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.

Status: Completed

Product Quantity: 1 unit

Code Information:

Serial Number: PA7940RGG5130514B; UDI: 0100850038247027211001077

Distribution Pattern:

US: NY OUS: None

Voluntary or Mandated:

Voluntary: Firm initiated