FDA Device recall Z-1369-2013
Shimadzu Corporation - Mobile DaRt Evolution This device is a mobile X-ray system in order to take general radiography of patients in the h…
- FDA Device
- Class II
- terminated
- Published 2013-06-12
On 2013-06-12 the FDA classified a Class II recall of Shimadzu Corporation - Mobile DaRt Evolution This device is a mobile X-ray system in order to take general radiography of patients in the h… by Shimadzu Medical Systems, citing the recall was initiated because Shimadzu Corporation has identified a potential issue in certain manufacturing lots of the Shimadzu MobileDaRt Evolution in combination with CXDI-….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1369-2013 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-03-18 |
| Published | 2013-06-12 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Shimadzu Medical Systems |
| Distribution | US |
Product
Shimadzu Corporation - Mobile DaRt Evolution This device is a mobile X-ray system in order to take general radiography of patients in the hospital who cannot move and/or of out patients in emergency .
Reason
The recall was initiated because Shimadzu Corporation has identified a potential issue in certain manufacturing lots of the Shimadzu MobileDaRt Evolution in combination with CXDI-70C, CXDI-55C, and CXDI-55G. As a result of Shimadzu's investigation, there is a potential risk for screws becoming loose inside the Shimadzu Mobile X-ray systems.
Identifiers
| code_info | In combination with CXDI-70C: Serial Numbers: 410001F0A004 410001B13012 410001B13016 410001F0A005 410001B1300…In combination with CXDI-70C: Serial Numbers: 410001F0A004 410001B13012 410001B13016 410001F0A005 410001B1300E 410001B13010 0162S67303 410001B13018 410001B1300A 410001B13017 410001B1301B 410001B1301A 410001B13019 410001B1301D 410001B13011 410001B1301C 410001B13001 410001B13015 410001F0B004 410001B13008 410001B13013 410001F0B005 410001F0B006 410001F0A007 410001B13009 410001B1300B 410001B15035 410001B13014 410001B14009 410001B1301F 410001B14002 410001B14001 410001B14006 410001B14004 410001B15005 410001B13002 410001B1301E 410001B15016 410001B15009 410001B15007 410001B15006 410001B1300F 410001B15001 410001B15017 410001B15002 410001B15020 In combination with CXDI-55C: Serial Numbers: 0162S65805 0162S65810 0162S65808 0162S66001 0162S66008 0162S65809 0162S66004 0162S66005 0162S66009 0162S66010 0162S66201 0162S66202 0162S66207 0162S66208 0162S66206 0162S66302 0162S66402 0162S66409 0162S66410 0162S66403 0162S66501 |
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Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1369-2013%22
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