🔍 RecallPedia

Various models of BD Pyxis Pro 7-Drawer Auxiliary, Reference numbers: 1149-00 and 1152-00

Class I - Dangerous
🏥 Medical Devices Recalled: September 30, 2025 CareFusion 303 Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    All Serial Numbers/Ref #/UDI: 1149-00 10885403517822 and 1152-00 10885403517839
  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:
Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire.
Classification:
Class I - Dangerous

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

Status:
ongoing

Product Information

Full Description:

Various models of BD Pyxis Pro 7-Drawer Auxiliary, Reference numbers: 1149-00 and 1152-00

Product Codes/Lot Numbers:

All Serial Numbers/Ref #/UDI: 1149-00 10885403517822 and 1152-00 10885403517839

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0369-2026

Related Recalls