RelieVR REF: RVX-2002, Rx Only. Virtual reality behavioral therapy device for pain relief.
This recall has been completed (originally issued June 30, 2023).
- Company
- Appliedvr
- Recall Initiated
- February 27, 2023
- Posted
- June 30, 2023
- Recall Number
- Z-2044-2023
- Quantity
- 1 unit
- Firm Location
- Van Nuys, CA
- Official Source
- View on FDA website ↗
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.
Distribution
US: NY OUS: None
Lot / Code Info
Serial Number: PA7940RGG5130514B; UDI: 0100850038247027211001077
Root Cause
Software Manufacturing/Software Deployment
Action Taken
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.