FDA Medical Device Recalls (openFDA)
Appliedvr: RelieVR REF: RVX-2002, Rx Only. Virtual reality behavioral therapy device for pain relief.
- Recall number
- Z-2044-2023
- Recalling firm
- Appliedvr
- Product
- RelieVR REF: RVX-2002, Rx Only. Virtual reality behavioral therapy device for pain relief.
- Status
- Completed
- Initiated
- 2023-02-27
- Posted
- 2023-06-30
- Terminated
- not on file
- Reason
- There is the potential for the program software to malfunction which will not allow it to move forward to the next session.
- Root cause
- Software Manufacturing/Software Deployment
- 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.
- Quantity
- 1 unit
- Distribution
- US: NY OUS: None
- Lot, serial or model codes
- Serial Number: PA7940RGG5130514B; UDI: 0100850038247027211001077
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- QRA
- Firm FEI
- 3021071568
- Firm city
- Van Nuys
- Firm state
- CA
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28