Reported Oct 12, 2016 · Terminated

Ingenuity CT Model Number 728326 Product Usage: Computed Tomography X-ray systems intended to product cross-sectional…

Philips Medical Systems

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Philips Medical Systems · 595 Miner Rd · Cleveland, OH · 44143-2131

Is this the product you have?

  • Ingenuity
  • CT Model Number 728326 Product UsageComputed Tomography X-ray systems intended to product cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes
Lot codes and dates
  • 233 of 233 codes

    • 30003
    • 30004
    • 30005
    • 30006
    • 30007
    • 30008
    • 30009
    • 30010
    • 30011
    • 30012
    • 30013
    • 30014
    • 30015
    • 30017
    • 30018
    • 30019
    • 30020
    • 30021
    • 30022
    • 30025
    • 30026
    • 30027
    • 30028
    • 30029
    • 30030
    • 30031
    • 30032
    • 30033
    • 30034
    • 30036
    • 30037
    • 30038
    • 30039
    • 30040
    • 30041
    • 30042
    • 30043
    • 30044
    • 30045
    • 30046
    • 30047
    • 30049
    • 32045
    • 32083
    • 32107
    • 52051
    • 52060
    • 52062
    • 300003
    • 300004
    • 300005
    • 300009
    • 300010
    • 300011
    • 300012
    • 300013
    • 300014
    • 300015
    • 300016
    • 300017
Amount recalled
235

This recall covers 4 products

The agency filed one notice per product. You are reading one of them; the other 3 are below.

Where it was sold

Why it was recalled

The infant performance test did not meet the test specification for the Infant Head Uniformity test with High Resolution. As a result, when the user performs High Resolution head scans, the reconstructed images may exhibit degraded image quality manifested as non-uniformity of the image, CT number shift greater than 5 Hounsfield units, and reduction in gray/white matter differentiation. The issue is most sever in the High Resolution mode, and the factory reference pediatric scan protocols are set to High Resolution default. Adults head scans have a factory reference protocol that defaults to standard resolution which doesn't experience the issue.

This product could cause temporary or reversible health problems — stop using it.

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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Jul 2, 2018 · Data as of Sep 19, 4:15 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.