🔍 RecallPedia

Ingenia Ambition X, Model No. 782109

Class I - Dangerous
🏥 Medical Devices Recalled: December 29, 2023 Philips North America Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    Model No. 782109 UDI-DI 00884838098350 Serial Number 47785
  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:
An incorrect electrical shock warning label may have been placed on the Liquid Cooling Cabinet (LCC) of affected MR systems. The caution symbol on the incorrect label has a white background instead of yellow, and the label is missing the high voltage warning symbol. This presents a potential risk of electrical shock for service personnel.
Classification:
Class I - Dangerous

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

Status:
ongoing

Product Information

Full Description:

Ingenia Ambition X, Model No. 782109

Product Codes/Lot Numbers:

Model No. 782109 UDI-DI 00884838098350 Serial Number 47785

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0810-2024

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