MX8000IDT CT Scanner using version 2.5.5, 3.0, 3.1, 3.2, 3.2.2, or 3.2.4 software.
FDA device recall Z-1413-05 · posted 2005-08-30 · Terminated
Recall details
- Recalling firm
- Philips Medical Systems (Cleveland) Inc
- Reason for recall
- When two product applications called Flip and Secondary Capture are used together, it is possible for image orientation labels to be incorrect.
- Action taken
- The firm sent recall/field correction letters dated 3/11/05.
- Root cause
- Other
- Status
- Terminated
- Product code
- JAK
- Distribution
- The devices were distributed to consignees throughout the United States and to consigness located in Argentina, Austria, Bahama, Belarus, Belguim, Brazil, Canada, China, Chile, Columbia, Costa Rica, C
- Date initiated
- 2005-03-11
- Date posted
- 2005-08-30
- Date terminated
- 2012-03-02
- Location
- Cleveland, OH
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