RelieVR recall: Software Issue
RelieVR REF: RVX-2002, Rx Only. Virtual reality behavioral therapy device for pain relief.
Why was RelieVR recalled?
There is the potential for the program software to malfunction which will not allow it to move forward to the next session.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Serial Number: PA7940RGG5130514B; UDI: 0100850038247027211001077
- Product
- RelieVR REF: RVX-2002, Rx Only. Virtual reality behavioral therapy device for pain relief.
- Recalling firm
- Appliedvr
- Quantity
- 1 unit
- Distribution
- US: NY OUS: None
- Recall date
- July 5, 2023
- Classification
- Class II
- Status
- Completed
- Agency
- FDA (device)