🔍 RecallPedia

BD Care Coordination Engine (CCE) Infusion Adapter, Safety Management Software

Class I - Dangerous
🏥 Medical Devices Recalled: February 18, 2025 CareFusion 303 Infusion Pumps Nationwide

What Should You Do?

  1. Check if you have this product:
    Software: v1.7.2/UDI: 10885403510472
  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:
CareFusion 303, Inc.
Reason for Recall:
Software issue that may result in outdated automated programming request(APR) being sent to the progressive care unit (PCU).
Classification:
Class I - Dangerous

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

Status:
ongoing

Product Information

Full Description:

BD Care Coordination Engine (CCE) Infusion Adapter, Safety Management Software

Product Codes/Lot Numbers:

Software: v1.7.2/UDI: 10885403510472

Distribution:

Nationwide distribution

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1305-2025

Related Recalls