🔍 RecallPedia

BD PYXIS MEDBANK TWR MN CR-8HH-3FH-P, REF: 169-98 containing software version 3.9.1.9

Class I - Dangerous
🏥 Medical Devices Recalled: June 24, 2024 CareFusion 303 Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    UDI: 10885403512568/ Serial Number: 16261297
  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 software issue, there is a potential when a restock label is printed for a medication stored in automated dispensing cabinets, that the incorrect bin for the medication is printed on the label.
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 TWR MN CR-8HH-3FH-P, REF: 169-98 containing software version 3.9.1.9

Product Codes/Lot Numbers:

UDI: 10885403512568/ Serial Number: 16261297

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-2502-2024

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