🔍 RecallPedia

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

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 Numbers: (1) 782116, (2) 782148; UDI-DI: (1) 00884838099722, (2) 00884838108714; Serial Numbers: (1) 41042, 41047, 41080, 41139, 41229, 41287, 41295, 41327, 41367, 41424, 41432, 41433, 41457, 41568, 70068, 70284, 70630, 70696, 70995, 70996, 81021, (2) 41011, 41031, 41244, 41284, 41334, 41427, 41464, 41488, 41523, 41534, 41547, 70067, 70289, 70452, 70454, 70473, 70590, 70622, 70644, 70652, 70742, 70769, 70803, 70829, 70966, 70980, 84102, 84109, 84368, 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 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: Evolution Upgrade 1.5T; Model Numbers: (1) 782116, (2) 782148;

Product Codes/Lot Numbers:

Model Numbers: (1) 782116, (2) 782148; UDI-DI: (1) 00884838099722, (2) 00884838108714; Serial Numbers: (1) 41042, 41047, 41080, 41139, 41229, 41287, 41295, 41327, 41367, 41424, 41432, 41433, 41457, 41568, 70068, 70284, 70630, 70696, 70995, 70996, 81021, (2) 41011, 41031, 41244, 41284, 41334, 41427, 41464, 41488, 41523, 41534, 41547, 70067, 70289, 70452, 70454, 70473, 70590, 70622, 70644, 70652, 70742, 70769, 70803, 70829, 70966, 70980, 84102, 84109, 84368, 84630, 84825;

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1793-2025

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