🔍 RecallPedia

Evolution Upgrade 3.0T Model Numbers (REF): (1) 782117, (2) 782143;

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 Numbers (REF): (1) 782117, (2) 782143; UDI-DI: (1) 00884838099739, (2) 00884838108660; Serial Numbers: (1) 42003, 42023, 42024, 42029, 42078, 42217, 42246, 42375, 42402, 42408, 71044, 71348, 71774, 85146, 85645, 85663, 85668, 85675, 85677, 85680, 85685, 85687, 85694, 85698, 85705, 85713, (2) 3, 42069, 42193, 42225, 42308, 42320, 42366, 42415, 71595, 71815, 71836, 85649, 85651, 85682, 85683, 85684, 85688, 85690, 85695, 85697, 85699, 85701, 85708, 85714;
  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:

Evolution Upgrade 3.0T Model Numbers (REF): (1) 782117, (2) 782143;

Product Codes/Lot Numbers:

Model Numbers (REF): (1) 782117, (2) 782143; UDI-DI: (1) 00884838099739, (2) 00884838108660; Serial Numbers: (1) 42003, 42023, 42024, 42029, 42078, 42217, 42246, 42375, 42402, 42408, 71044, 71348, 71774, 85146, 85645, 85663, 85668, 85675, 85677, 85680, 85685, 85687, 85694, 85698, 85705, 85713, (2) 3, 42069, 42193, 42225, 42308, 42320, 42366, 42415, 71595, 71815, 71836, 85649, 85651, 85682, 85683, 85684, 85688, 85690, 85695, 85697, 85699, 85701, 85708, 85714;

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-2203-2025

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