Reported Jun 10, 2026 · Ongoing

Digital Angiography System Trinias:UD150G-40 / D150GC-40; Digital Angiography System BRANSIST safire:UD150G-40 /…

Shimadzu Medical Systems

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Shimadzu Medical Systems · 3645 N Lakewood Blvd · Long Beach, CA · 90808-1797

Is this the product you have?

13 of 13 products

Products covered by this recall
#Product as published
1Digital Angiography System Trinias:UD150G-40 / D150GC-40
2Digital Angiography System BRANSIST safire:UD150G-40 / D150GC-40
3Digital Angiography System BRANSIST alexa:UD150G-40 / D150GC-40
4Digital Radiography System RADspeed Pro: UD150B-40 / UD150V-40 / UD150L-40 / UD150L-40E/D150BC-40 / D150VC-40 / D150LC-40 / D150LC-40E/D150BC-41 / D150VC-41 / D150LC-41
5Digital Radiography System RADspeed safire: UD150B-40 / D150BC-40
6Radiography System RADspeed fit: N/A (Integrated in the system)
7X-RAY R/F SYSTEM SONIALVISION safire17:UD150B-40 / D150BC-40
8X-RAY R/F SYSTEM SONIALVISION safire Plus: UD150B-40 / D150BC-4
90 X-RAY R/F SYSTEM SONIALVISION safire: UD150B-40 / D150BC-40
10X-RAY R/F SYSTEM SONIALVISION VERSA: UD150B-40 / UD150V-40 / UD150L-40/D150BC-40 / D150VC-40 / D150LC-40
11X-RAY R/F SYSTEM FLUOROspeed 300:UD150B-40 / UD150V-40 / UD150L-40/D150BC-40 / D150VC-40 / D150LC-40
12X-RAY R/F SYSTEM SONIALVISION G4:D150BC-40S
13X-RAY R/F SYSTEM FLUOROspeed X1:D150BC-40S
Lot codes and dates
  • System Serial Numbers

    2,715 of 2,715 codes

    • SMS20080542
    • SMS20120038
    • SMS20140084
    • SMS20090038
    • SMSMA110013
    • SMS20090239
    • SMS20080581
    • SMS20090099
    • SMS20110202
    • SMS2010011
    • SMS20080609
    • SMS20100127
    • SMS20090157
    • SMS20080573
    • SMS20100230
    • SMSMA130031
    • SMS20105020
    • SMS20080009
    • SMS20080174
    • SMS20090316
    • SMS20090281
    • SMSMA100027
    • SMSHP100002
    • SMSHP100001
    • SMS20100007
    • SMSHP100013
    • SMS20100068
    • SMS20100010
    • SMSBL110013
    • SMSMA120007
    • SMSNO130066
    • SMSHP110014
    • SMSMA130015
    • SMSPR130007
    • SMSBL120003
    • SMSMA110022
    • SMSNO120020
    • SMS20130105
    • SMS20160046
    • SMSVZ160014
    • SMS20080264
    • SMS20170160
    • SMS20160049
    • SMS20080358
    • SMS20080519
    • SMS20080238
    • SMS20080135
    • SMS20080493
    • SMS20090134
    • SMS20085122
    • SMS20070007
    • SMS20070013
    • SMS20095174
    • SMS20080128
    • SMS20210210
    • SMS20080283
    • SMS20080284
    • SMS20080154
    • SMS20170211
    • SMS20080091
    SM
Amount recalled
3487 units

Where it was sold

Why it was recalled

Electromagnetic contactors within high voltage generator may weld together, resulting in current being supplied to power supply even if power is off.

This product could cause temporary or reversible health problems — stop using it.

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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 3:26 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.