🔍 RecallPedia

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

Class I - Dangerous
🏥 Medical Devices Recalled: February 27, 2023 Appliedvr Other Medical Devices

What Should You Do?

  1. Check if you have this product:
    Serial Number: PA7940RGG5130514B; UDI: 0100850038247027211001077
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
Appliedvr
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.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
completed

Product Information

Full Description:

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

Product Codes/Lot Numbers:

Serial Number: PA7940RGG5130514B; UDI: 0100850038247027211001077

Distribution:

Distributed in: US, NY

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-2044-2023