🔍 RecallPedia

SmartPath to dStream for 3.0T Model Number (REF): 782145;

Class I - Dangerous
🏥 Medical Devices Recalled: June 30, 2025 Philips North America Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    Model Number (REF): 782145; UDI-DI: 00884838108684; Serial Numbers: 17377, 17385, 17435, 34114, 34208, 38118, 38127, 38170, 38294, 38313, 38336, 73002, 73004, 74002, 74004;
  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:
The potential for component failures in the Gradient Coil of the affected MR systems may act as a heat source with a potential to produce smoke and/or fire.
Classification:
Class I - Dangerous

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

Status:
ongoing

Product Information

Full Description:

SmartPath to dStream for 3.0T Model Number (REF): 782145;

Product Codes/Lot Numbers:

Model Number (REF): 782145; UDI-DI: 00884838108684; Serial Numbers: 17377, 17385, 17435, 34114, 34208, 38118, 38127, 38170, 38294, 38313, 38336, 73002, 73004, 74002, 74004;

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-2215-2025

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