🔍 RecallPedia

Evolution Upgrade 1.5T Model Numbers (REF): (1) 782116, (2) 782148;

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) 782116, (2) 782148; UDI-DI: (1) 00884838099722, (2) 00884838108714; Serial Numbers: (1) 41017, 41024, 41025, 41041, 41042, 41047, 41051, 41080, 41089, 41130, 41139, 41143, 41144, 41179, 41189, 41196, 41226, 41229, 41235, 41286, 41287, 41295, 41311, 41327, 41344, 41349, 41367, 41413, 41424, 41432, 41433, 41457, 41491, 41497, 41520, 41527, 41568, 70068, 70093, 70099, 70190, 70202, 70205, 70260, 70284, 70589, 70630, 70696, 70949, 70995, 70996, 81021, 81073, 84370, 84741, (2) 41011, 41031, 41182, 41244, 41277, 41284, 41334, 41392, 41427, 41446, 41464, 41488, 41523, 41534, 41547, 70067, 70289, 70452, 70454, 70473, 70590, 70596, 70622, 70644, 70652, 70742, 70769, 70803, 70829, 70966, 70980, 70983, 84102, 84109, 84368, 84435, 84630, 84825,
  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 1.5T Model Numbers (REF): (1) 782116, (2) 782148;

Product Codes/Lot Numbers:

Model Numbers (REF): (1) 782116, (2) 782148; UDI-DI: (1) 00884838099722, (2) 00884838108714; Serial Numbers: (1) 41017, 41024, 41025, 41041, 41042, 41047, 41051, 41080, 41089, 41130, 41139, 41143, 41144, 41179, 41189, 41196, 41226, 41229, 41235, 41286, 41287, 41295, 41311, 41327, 41344, 41349, 41367, 41413, 41424, 41432, 41433, 41457, 41491, 41497, 41520, 41527, 41568, 70068, 70093, 70099, 70190, 70202, 70205, 70260, 70284, 70589, 70630, 70696, 70949, 70995, 70996, 81021, 81073, 84370, 84741, (2) 41011, 41031, 41182, 41244, 41277, 41284, 41334, 41392, 41427, 41446, 41464, 41488, 41523, 41534, 41547, 70067, 70289, 70452, 70454, 70473, 70590, 70596, 70622, 70644, 70652, 70742, 70769, 70803, 70829, 70966, 70980, 70983, 84102, 84109, 84368, 84435, 84630, 84825,

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-2202-2025

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