🔍 RecallPedia

ARIA Radiation Therapy Management (RTM) VERSIONS 13.6, 15.1, 15.5, 15.6, 16.0, 16.1

Class I - Dangerous
🏥 Medical Devices Recalled: March 21, 2022 Varian Medical Systems Imaging Laboratory GmbH Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    DI Numbers: 00856100006066, 00856100006080, 00856100006097, 00856100006110, 00856100006127,00856100006165
  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:
Varian Medical Systems Imaging Laboratory GmbH
Reason for Recall:
Software issue for treatment plan and image management application may result in mismatch values which could result in treatment in the wrong location
Classification:
Class I - Dangerous

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

Status:
completed

Product Information

Full Description:

ARIA Radiation Therapy Management (RTM) VERSIONS 13.6, 15.1, 15.5, 15.6, 16.0, 16.1

Product Codes/Lot Numbers:

DI Numbers: 00856100006066, 00856100006080, 00856100006097, 00856100006110, 00856100006127,00856100006165

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0942-2022