Philips Medical Systems (Cleveland) Inc Philips MX8000 IDT CT Scanner, utilizing V2.1 software. Recall
Hazard assessment based on recall description.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Philips MX8000 IDT CT Scanner, utilizing V2.1 software.
Brand
Philips Medical Systems (Cleveland) Inc
Lot Codes / Batch Numbers
Serial Numbers: 3094 through 3196.
Products Sold
Serial Numbers: 3094 through 3196.
Philips Medical Systems (Cleveland) Inc is recalling Philips MX8000 IDT CT Scanner, utilizing V2.1 software. due to Patient images may be incorrectly stored in the archive directory of a different patient.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Patient images may be incorrectly stored in the archive directory of a different patient.
Recommended Action
Per FDA guidance
The firm mailed a ''Product Safety Notification'', dated 4/2/2003, to all affected user sites.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026