🔍 RecallPedia

BD Pyxis MedStation ES (Med ES Main), REF: 323; and BD Pyxis MedStation ES (Med ES Main Tower), REF: 352

Class I - Dangerous
🏥 Medical Devices Recalled: April 5, 2023 CareFusion 303 Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    Software v1.7.3. REF/UDI-DI: 323/10885403512667, 352/10885403512674
  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:
Due to an automated dispensing cabinet software issue, when a medication single order contains more than one component and at least one is unavailable for a multi-item or combination order, the order may display as grayed out; alternate location tooltip will display "Server connection failed," not listing other area devices where unavailable item(s) may be found, which may lead to delayed therapy.
Classification:
Class I - Dangerous

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

Status:
ongoing

Product Information

Full Description:

BD Pyxis MedStation ES (Med ES Main), REF: 323; and BD Pyxis MedStation ES (Med ES Main Tower), REF: 352

Product Codes/Lot Numbers:

Software v1.7.3. REF/UDI-DI: 323/10885403512667, 352/10885403512674

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0906-2025

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