🔍 RecallPedia

Change Healthcare Cardiology Hemo software

Class I - Dangerous
🏥 Medical Devices Recalled: December 2, 2024 A L I Technologies Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    Software version/UDI: 14.1.1/(01)17540262100020, 14.2/(01)17540262100037, 14.3/(01)17540262100044, 14.3.2/(01)17540262100051, 15.01/(01)17540262100105, 15.1/(01)17540262100129
  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:
A L I Technologies Ltd
Reason for Recall:
Software defect concerning autosave mechanism may result in the clinician administering incorrect medication(s).
Classification:
Class I - Dangerous

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

Status:
ongoing

Product Information

Full Description:

Change Healthcare Cardiology Hemo software

Product Codes/Lot Numbers:

Software version/UDI: 14.1.1/(01)17540262100020, 14.2/(01)17540262100037, 14.3/(01)17540262100044, 14.3.2/(01)17540262100051, 15.01/(01)17540262100105, 15.1/(01)17540262100129

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0958-2025

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