🔍 RecallPedia

Product Name: Ingenia 3.0T CX; Model Number: 781271;

Class I - Dangerous
🏥 Medical Devices Recalled: May 13, 2025 Philips North America Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    Model Number: 781271; UDI-DI: 00884838068452; Serial Numbers: 78012, 78016, 78017, 78018, 78025, 78028, 78033, 78035, 78039, 78042, 78045, 78050, 78053, 78060, 78062, 78082, 78095, 78100, 78112, 78122, 78123, 78133, 78147, 78148, 78155, 78175, 78197, 78199, 78201, 78202, 78217, 78229, 78239, 78259, 78260, 78286, 78287;
  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 Llc
Reason for Recall:
Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.
Classification:
Class I - Dangerous

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

Status:
ongoing

Product Information

Full Description:

Product Name: Ingenia 3.0T CX; Model Number: 781271;

Product Codes/Lot Numbers:

Model Number: 781271; UDI-DI: 00884838068452; Serial Numbers: 78012, 78016, 78017, 78018, 78025, 78028, 78033, 78035, 78039, 78042, 78045, 78050, 78053, 78060, 78062, 78082, 78095, 78100, 78112, 78122, 78123, 78133, 78147, 78148, 78155, 78175, 78197, 78199, 78201, 78202, 78217, 78229, 78239, 78259, 78260, 78286, 78287;

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1800-2025

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