🔍 RecallPedia

BD Pyxis MedBank MedPass Software, REF: 139088-01

Class I - Dangerous
🏥 Medical Devices Recalled: August 18, 2023 CareFusion 303 Other Medical Devices

What Should You Do?

  1. Check if you have this product:
    UDI-DI: 10885403513817, Software versions prior to but not including v1.2.3.23
  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:
After dispensing a timed dose medication for a patient, the automated dispensing cabinet software may continue to show the already dispensed medication dose is still available for dispense, which could lead to duplicate medication administration.
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 MedBank MedPass Software, REF: 139088-01

Product Codes/Lot Numbers:

UDI-DI: 10885403513817, Software versions prior to but not including v1.2.3.23

Distribution:

Distributed in: US, FL, MI, KS

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-2646-2023

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