🔍 RecallPedia

Philips Incisive CT -Computed Tomography X-Ray System Model Number: 72813

Class I - Dangerous
🏥 Medical Devices Recalled: March 20, 2023 Philips North America Infusion Pumps Nationwide

What Should You Do?

  1. Check if you have this product:
    UDI-DI:(01)00884838085015(21) + Serial number US Serial Numbers: 33041, 500301, 500252. OUS Serial Numbers: 33040, 500408
  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:
Philips North America
Reason for Recall:
Multi-Function Foot Switch Unload Pedal Foot Entrapment-Pressing the Unload Pedal of the foot switch to perform the unload function may cause entrapment of the operator's foot and injury
Classification:
Class I - Dangerous

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

Status:
ongoing

Product Information

Full Description:

Philips Incisive CT -Computed Tomography X-Ray System Model Number: 72813

Product Codes/Lot Numbers:

UDI-DI:(01)00884838085015(21) + Serial number US Serial Numbers: 33041, 500301, 500252. OUS Serial Numbers: 33040, 500408

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1586-2023

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