Arcadis Orbic Mobile X-Ray System
FDA Recall Z-0438-06 · Posted 2006-01-25
Recalling FirmSiemens Medical Solutions USA, Inc
Recall StatusTerminated
Product CodeJAK
Date Initiated2005-12-12
Date Terminated2008-09-04
Product Quantity179 units
Reason for Recall
patient information can be stored in another patient's file.
Firm Action
The recalling firm has issued a Customer Safety Advisory to the affected customers per Update Instructions SP030/05/S. The letter informs customers of the potential problem and provides a suggestion to avoid this issue.
Root Cause
Other
Distribution Pattern
The product was shipped to medical facilities nationwide.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.