Severity
Moderate
ModerateClass IIOngoing
FDA Devices recall · Reported February 14, 2024
Spectral CT 7500: Software Version 5.0, Model 728333 and Spectral CT 7500 China: Software Version 5.0, Model 728340.
A software issue that can incorrectly label all captured images that may lead to misdiagnosis and subsequent incorrect treatment.
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
Philips Medical Systems recalled Spectral CT 7500: Software Version 5.0, Model 728333 and Spectral CT 7500 China: Software… - a moderate-severity action.
Spectral CT 7500: Software Version 5.0, Model 728333 and Spectral CT 7500 China: Software… was recalled by Philips Medical Systems in February 14, 2024. Reason: A software issue that can incorrectly label all captured images that may lead to misdiagnosis and subsequent …. Check the official notice for the remedy. Verify recall #Z-1055-2024 with the FDA Devices before acting.
The recall
Philips Medical Systems issued this moderate-severity FDA Devices recall-A software issue that can incorrectly label all captured images that may lead to misdiagnosis and subsequent ….
- Moderate
- severity level
- Class II
- classification
- February 14, 2024
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-1055-2024 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-1055-2024) was formally reported on February 14, 2024, with the manufacturer initiating the action on December 13, 2023. It is classified under Moderate severity (Class II), with a current status of Ongoing. Philips Medical Systems is listed as the recalling firm, operating out of Cambridge, MA. Federal records list the affected scope as US: 33, OUS 177.
The documented reason for this recall is: A software issue that can incorrectly label all captured images that may lead to misdiagnosis and subsequent incorrect treatment. Distribution data in the federal record shows the product reached: Worldwide - US Nationwide distribution in the states of AR, AZ, GA, HI, IN, KY, MA, MD, MN, NY, OH, PA, TX & WV; the countries of Australia, Austria, Belgium, China, Czech Republic, Denmark, Germany, Israel, Italy, Jap…. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 3 from FDA Devices - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Medical Devices recalls over time
Where this recall sits in its category - 40,322 medical devices recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
US: 33, OUS 177
Related Recalls
6
3 from same agency
Product description
Spectral CT 7500: Software Version 5.0, Model 728333 and Spectral CT 7500 China: Software Version 5.0, Model 728340.
Reason for recall
A software issue that can incorrectly label all captured images that may lead to misdiagnosis and subsequent incorrect treatment.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Ongoing |
| Recall number | Z-1055-2024 |
| Date reported | February 14, 2024 |
| Date initiated | December 13, 2023 |
| Recalling firm | Philips Medical Systems |
| Firm location | Cambridge, MA |
| Affected scope | US: 33, OUS 177 |
| Distribution | Worldwide - US Nationwide distribution in the states of AR, AZ, GA, HI, IN, KY, MA, MD, MN, NY, OH, PA, TX & WV; the countries of Australia, Austria, Belgium, China, Czech Republic, Denmark, Germany, Israel, Italy, Japan, Macao, Malaysia,… |
Profile values are sourced directly from the official FDA Devices enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (Z-1055-2024) and product description against the item you own. Search the archive
- Confirm the current status with FDA Devices before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Devices record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
Spectral CT 7500: Software Version 5.0, Model 728333 and Spectral CT 7500 China: Software Version 5.0, Model 728340.. Recalled by Philips Medical Systems. Units affected: US: 33, OUS 177.
Why was this product recalled? ▼
A software issue that can incorrectly label all captured images that may lead to misdiagnosis and subsequent incorrect treatment.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on February 14, 2024. Severity: Moderate. Recall number: Z-1055-2024.
Where was the recalled product distributed? ▼
Distribution: Worldwide - US Nationwide distribution in the states of AR, AZ, GA, HI, IN, KY, MA, MD, MN, NY, OH, PA, TX & WV; the countries of Australia, Austria, Belgium, China, Czech Republic, Denmark, Germany, Israel, Italy, Japan, Macao, Malaysia, Netherlands, Norway, Palestine, Panama, Portugal, Singapore, South Korea, Spain, Switzerland, Taiwan, Thailand & United Kingdom..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-1055-2024) against your product. Visit the official FDA Devices website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device? ▼
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Devices, reported February 14, 2024. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.