🔍 RecallPedia

Intera 0.5T Standard, Magnetic Resonance System.

Class I - Dangerous
🏥 Medical Devices Recalled: March 12, 2024 Philips North America Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    Model No. 781101; UDI-DI n/a; Serial No. 6047, 6018, 6023, 6027, 6031, 6044, 6060, 10306, 6015, 6061, 6025, 6054, 6001, 6066.
  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:
Patient support table floor plate may be incorrectly installed.
Classification:
Class I - Dangerous

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

Status:
ongoing

Product Information

Full Description:

Intera 0.5T Standard, Magnetic Resonance System.

Product Codes/Lot Numbers:

Model No. 781101; UDI-DI n/a; Serial No. 6047, 6018, 6023, 6027, 6031, 6044, 6060, 10306, 6015, 6061, 6025, 6054, 6001, 6066.

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1572-2024

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