MOSAIQ Oncology Information System The product is used to manage workflows for treatment planning and delivery. It supports information flow among healthcare facility personnel and can be use wherever radiotherapy and chemotherapy are prescribed.

Class I - Dangerous
πŸ₯ Medical Devices Recalled: December 2, 2016 Elekta Infusion Pumps Nationwide

What Should You Do?

  1. Check if you have this product:
    Versions 2.60 an higher
  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:
Elekta, Inc.
Reason for Recall:
Edits to Particle field definition parameters may not be saved when the field definition window is saved.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

MOSAIQ Oncology Information System The product is used to manage workflows for treatment planning and delivery. It supports information flow among healthcare facility personnel and can be use wherever radiotherapy and chemotherapy are prescribed.

Product Codes/Lot Numbers:

Versions 2.60 an higher

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0731-2017

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