🔍 RecallPedia

IQon Spectral CT - Model no. 728332, Computed Tomography X-Ray system Product Usage: Computed Tomography X-ray systems intended to produce cross-sectional Images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes. These devices may include signal analysts and display equipment, patient and equipment supports, components, and accessories.

Class I - Dangerous
🏥 Medical Devices Recalled: February 8, 2018 Philips Medical Systems (Cleveland) Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    Serial no: 860023 860035 860047 860059 860010 860014 860015 860013 860029 860006 860002 860061 860011 860020 860024 860008 860039 860043 860018 860012 860022 860032 860033 860040 860009 860016 860017 860042 860003 860005 860037 860041 860025 860038 860036 860052 860056 860021 860053 860019 860054 860044 860028 860030 860026 860031 860034
  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 Medical Systems (Cleveland) Inc
Reason for Recall:
Closing the Emergency Stop may disable the horizontal motor, allowing the couch top to move during patient load or unload activities.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

IQon Spectral CT - Model no. 728332, Computed Tomography X-Ray system Product Usage: Computed Tomography X-ray systems intended to produce cross-sectional Images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes. These devices may include signal analysts and display equipment, patient and equipment supports, components, and accessories.

Product Codes/Lot Numbers:

Serial no: 860023 860035 860047 860059 860010 860014 860015 860013 860029 860006 860002 860061 860011 860020 860024 860008 860039 860043 860018 860012 860022 860032 860033 860040 860009 860016 860017 860042 860003 860005 860037 860041 860025 860038 860036 860052 860056 860021 860053 860019 860054 860044 860028 860030 860026 860031 860034

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1414-2018

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Class I - Dangerous

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