Modularis URO urological table Model number 5531012
FDA Recall Z-0168-2007 · Posted 2006-11-14
Recalling FirmSiemens Medical Solutions USA, Inc
Recall StatusTerminated
Product CodeMMZ
Date Initiated2006-10-01
Date Terminated2008-05-13
Product Quantity59 units
Reason for Recall
Potential pinch point with the patient table
Firm Action
The recalling firm has issued a Customer Safety Advisory to affected customers per Update Instructions SPO23/06/S. This letter, to be inserted in the system Operator Manual, reminds customers of the potential pinch point and provides a suggestion to avoid its occurrence.
Root Cause
Other
Distribution Pattern
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.