FDA Device recall Z-1039-2019
SHIMADZU MobileDaRt Evolution (MX8 Version), Mobile X-Ray System Product Usage: This device is intended to be used to take a film, CR or ge…
- FDA Device
- Class II
- terminated
- Published 2019-03-27
On 2019-03-27 the FDA classified a Class II recall of SHIMADZU MobileDaRt Evolution (MX8 Version), Mobile X-Ray System Product Usage: This device is intended to be used to take a film, CR or ge… by Shimadzu Medical Systems Usa Com, citing in these units, the brake is usually released by gripping the drive handle and applied by letting go of the handle. However, for systems within a specified manufacture period, we….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1039-2019 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-01-14 |
| Published | 2019-03-27 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Shimadzu Medical Systems Usa Com |
| Distribution | US |
Product
SHIMADZU MobileDaRt Evolution (MX8 Version), Mobile X-Ray System Product Usage: This device is intended to be used to take a film, CR or general radiography of patients in the hospital who cannot move and/or of outpatients in emergency. Exposure can be captured on film, CR or Digital Radiography (DR).
Reason
In these units, the brake is usually released by gripping the drive handle and applied by letting go of the handle. However, for systems within a specified manufacture period, we have identified that even when letting go of the handle, the systems brakes are not applied. In this event, if the Operator releases the handle when the device is moving, the unit will continue to coast.
Identifiers
| code_info | Serial Numbers: S/N UDI 41F41DD7C001 (01)04540217059621(11)171214(21)41F41DD7C001 41F41DD7C002 (01)04540217059621(11…Serial Numbers: S/N UDI 41F41DD7C001 (01)04540217059621(11)171214(21)41F41DD7C001 41F41DD7C002 (01)04540217059621(11)171214(21)41F41DD7C002 41F41DD7C003 (01)04540217059621(11)171214(21)41F41DD7C003 41F41DD7C004 (01)04540217059621(11)171215(21)41F41DD7C004 41F41DD7C005 (01)04540217059621(11)171215(21)41F41DD7C005 41F41DD7C006 (01)04540217059621(11)171215(21)41F41DD7C006 41F41DD7C007 (01)04540217059621(11)171215(21)41F41DD7C007 41F41DD7C008 (01)04540217059621(11)171215(21)41F41DD7C008 41F41DD7C009 (01)04540217059621(11)171225(21)41F41DD7C009 41F41DD7C010 (01)04540217059621(11)171225(21)41F41DD7C010 41F41DD81001 (01)04540217059621(11)180115(21)41F41DD81001 41F41DD81002 (01)04540217059621(11)180115(21)41F41DD81002 41F41DD81003 (01)04540217059621(11)180116(21)41F41DD81003 41F41DD81004 (01)04540217059621(11)180116(21)41F41DD81004 41F41DD81005 (01)04540217059621(11)180117(21)41F41DD81005 41F41DD81006 (01)04540217059621(11)180118(21)41F41DD81006 41F41DD81007 (01)0454021705962 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1039-2019%22
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