Reported Jul 2, 2025 · Ongoing

Spectral CT. Computed tomography X-ray system.

Philips North America LLC

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 North America Llc · 222 Jacobs St · Cambridge, MA · 02141-2289

Is this the product you have?

  • Spectral CT. Computed tomography X-ray system.
Lot codes and dates
  • Part No. 728333
  • UDI

    585 of 585 codes

    • (01)00884838101111(21)10014
    • (01)00884838101111(21)10015
    • (01)00884838101111(21)10016
    • (01)00884838101111(21)10017
    • (01)00884838101111(21)10018
    • (01)00884838101111(21)10019
    • (01)00884838101111(21)10020
    • (01)00884838101111(21)10021
    • (01)00884838101111(21)10022
    • (01)00884838101111(21)10023
    • (01)00884838101111(21)10024
    • (01)00884838101111(21)10025
    • (01)00884838101111(21)10027
    • (01)00884838101111(21)10031
    • (01)00884838101111(21)10032
    • (01)00884838101111(21)10033
    • (01)00884838101111(21)10034
    • (01)00884838101111(21)10035
    • (01)00884838101111(21)10036
    • (01)00884838101111(21)10038
    • (01)00884838101111(21)10039
    • (01)00884838101111(21)10040
    • (01)00884838101111(21)10041
    • (01)00884838101111(21)10042
    • (01)00884838101111(21)10043
    • (01)00884838101111(21)10044
    • (01)00884838101111(21)10045
    • (01)00884838101111(21)10046
    • (01)00884838101111(21)10047
    • (01)00884838101111(21)10048
    • (01)00884838101111(21)10049
    • (01)00884838101111(21)10050
    • (01)00884838101111(21)10052
    • (01)00884838101111(21)10053
    • (01)00884838101111(21)10055
    • (01)00884838101111(21)10056
    • (01)00884838101111(21)10057
    • (01)00884838101111(21)10058
    • (01)00884838101111(21)10059
    • (01)00884838101111(21)10060
    • (01)00884838101111(21)10061
    • (01)00884838101111(21)10062
    • (01)00884838101111(21)10063
    • (01)00884838101111(21)10065
    • (01)00884838101111(21)10066
    • (01)00884838101111(21)10067
    • (01)00884838101111(21)10068
    • (01)00884838101111(21)10069
    • (01)00884838101111(21)10070
    • (01)00884838101111(21)10071
    • (01)00884838101111(21)10072
    • (01)00884838101111(21)10074
    • (01)00884838101111(21)10075
    • (01)00884838101111(21)10076
    • (01)00884838101111(21)10077
    • (01)00884838101111(21)10078
    • (01)00884838101111(21)10079
    • (01)00884838101111(21)10080
    • (01)00884838101111(21)10081
    • (01)00884838101111(21)10082
Amount recalled
370 units

Where it was sold

Why it was recalled

Devices with affected software may experience two unintended motion issues that may lead to contact between the Gantry or table with the operator or patient, along with additional software issues that affect CT performance.

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

Data as of Sep 19, 7:36 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.