Philips Medical Systems (Cleveland) Inc Philips Odyssey FX Workstations, used with Axis, Irix, or Meridian Gamma Camera Systems. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Philips Odyssey FX Workstations, used with Axis, Irix, or Meridian Gamma Camera Systems.
Brand
Philips Medical Systems (Cleveland) Inc
Lot Codes / Batch Numbers
All serial numbers / all models.
Products Sold
All serial numbers / all models.
Philips Medical Systems (Cleveland) Inc is recalling Philips Odyssey FX Workstations, used with Axis, Irix, or Meridian Gamma Camera Systems. due to Due to a software anomaly, an incorrect patient name may be transmitted with image to Odyssey workstation.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Due to a software anomaly, an incorrect patient name may be transmitted with image to Odyssey workstation.
Recommended Action
Per FDA guidance
The firm notified their affected consignees by letter on 9/15/2003. The customers were informed how to avoid the problem until a software upgrade is installed on the units.
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