--- title: "Digital Angiography System Trinias:UD150G-40 / D150GC-40; Digital Angiography... — FDA record Z-2294-2026 | Is It on Recall" description: "Electromagnetic contactors within high voltage generator may weld together, resulting in current being supplied to power supply even if power is off." url: https://isitonrecall.com/recall/fda-device-z-2294-2026-digital-angiography-system-trinias-ud150g-40-d150gc-40-digital-angiography-system-bransist-safire-ud/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement # Digital Angiography System Trinias:UD150G-40 / D150GC-40; Digital Angiography System BRANSIST safire:UD150G-40 / D150... — FDA record Z-2294-2026 Reported ongoing Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice. Source date Apr 20, 2026. Retrieved Oct 1, 2026. Last updated Oct 1, 2026. Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/). ## What the record says - **Product**: Digital Angiography System Trinias:UD150G-40 / D150GC-40; Digital Angiography System BRANSIST safire:UD150G-40 / D150GC-40; Digital Angiography System BRANSIST alexa:UD150G-40 / D150GC-40; Digital 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; Digital Radiography System RADspeed safire: UD150B-40 / D150BC-40; Radiography System RADspeed fit: N/A (Integrated in the system); X-RAY R/F SYSTEM SONIALVISION safire17:UD150B-40 / D150BC-40; X-RAY R/F SYSTEM SONIALVISION safire Plus: UD150B-40 / D150BC-4;0 X-RAY R/F SYSTEM SONIALVISION safire: UD150B-40 / D150BC-40; X-RAY R/F SYSTEM SONIALVISION VERSA: UD150B-40 / UD150V-40 / UD150L-40/D150BC-40 / D150VC-40 / D150LC-40; X-RAY R/F SYSTEM FLUOROspeed 300:UD150B-40 / UD150V-40 / UD150L-40/D150BC-40 / D150VC-40 / D150LC-40; X-RAY R/F SYSTEM SONIALVISION G4:D150BC-40S; X-RAY R/F SYSTEM FLUOROspeed X1:D150BC-40S - **Reason**: Electromagnetic contactors within high voltage generator may weld together, resulting in current being supplied to power supply even if power is off. - **Classification**: Class II - **Recalling firm**: Shimadzu Medical Systems - **Quantity**: 3487 units - **Agency-reported status**: Ongoing - **Source record identifier**: Z-2294-2026 [Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2294-2026%22) [What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice. ## Lot and product identifiers | Label field | Details supplied by the agency | | --- | --- | | Lot, code or applicability | System Serial Numbers: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 SMSHP110015 SMS20090136 SMS20120069 SMS20120023 SMSMA140083 SMS20140060 SMS20080332 SMS20080277 SMS20170376 SMSNO120066 SMS20160121 SMS20090086 SMS20080018 SMS20100098 SMS20100041 SMSBL110001 SMSMA130023 SMSHP130022 SMS20110205 SMS20170164 SMS20180266 SMS20170272 SMS20090054 SMS20060032 SMS20210085 SMS20080133 SMS20080155 SMS20110213 SMS20095208 SMSHP120011 SMS2012008 SMS20120094 SMS20120106 SMS20120107 SMSHP140009 SMSMA150070 SMS20140064 SMS20190264 SMS20100205 SMS20080189 SMS20100205 SMS20080190 SMS20070002 SMS20080162 SMS20100221 SMS20120011 SMS20110186 SMS20140003 SMS20090053 SMS20110139 SMS20095169 SMS20080247 SMS20090154 SMS20090039 SMSHP110007 SMS20200064 SMS20095200 SMS20080061 SMS20090188 SMS20090208 SMSVA090012 SMS20100114 SMS20100126 SMS20090214 SMS20090043 SMSMA110069 SMS20080156 SMS20190259 SMS20080109 SMS20070008 SMS20070001 SMS20210059 SMS20210193 SMS20210278 SMS20210392 SMS20210347 SMS20220070 SMS20220036 SMS20200068 SMS20200330 SMS20220168 SMS20220206 SMS20220299 SMS20220292 SMS20220323 SMS20220360 SMS20230010 SMS20230040 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SMS20080097 SMS20080096 SMS20080082 SMS20080083 SMS20080084 SMS20080086 SMS20080079 SMS20080080 SMS20080081 SMS20080125 SMS20080126 SMS20095127 SMS20230020 SMS20095131 SMS20095130 SMS20170036 SMS20170052 SMS20160213 SMS20095134 SMS20080457 SMS20080023 SMS20160062 SMS20160190 SMS20160197 SMS20160214 SMS20160212 SMS20090297 SMSBL100019 SMSBL110012 SMSHP110003 SMSMA110004 SMSMA110009 SMS20110068 SMS20100155 SMS20090246 SMS20090096 SMS20100184 SMS20100146 SMS20100001 SMS20100147 SMS20100025 SMS20100148 SMSMA100015 SMS20130114 SMS20120138 SMS20110146 SMS20130134 SMSNO130019 SMS20120114 SMSMA130011 SMSMA130019 SMSMA110020 SMSNO120006 SMSMA130052 SMS20120114 SMSBL120016 SMSNO130059 SMSNO120091 SMSHP110035 SMS20130031 SMSNO120096 SMS20130113 SMSNO130058 SMS20110144 SMS20110143 SMSMA130024 SMSMA130025 SMS20120059 SMSMA130020 SMSHP120008 SMS20130171 SMSNO120099 SMS20120064 SMS20110147 SMS20140011 SMSMA140006 SMS20140024 SMSNO130037 SMS20120073 SMSNO120053 SMS20110142 SMSNO130049 SMS20110145 SMS20110141 SMS20120093 SMSNO120039 SMSMA130062 SMSBL120009 SMSBL110031 SMSBL110032 SMS20130115 SMSBL110033 SMSVA140023 SMSCH120016 SMS20140056 SMSVA140014 SMS20130172 SMSMA140039 SMSMA120023 SMSHP160009 SMSNO150051 SMSHP160008 SMSMA140049 S... | The agency lot list is longer than this excerpt. [Read the complete list at the official source](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2294-2026%22). Match all identifying details in the current notice. A brand name alone is not enough. ## Distribution Worldwide - US Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, NE, NJ, NM, NV, NY, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, WA, WI, WV and the countries of Canada, The Bahamas, China, Denmark, Haiti. States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address. - [Alaska](https://isitonrecall.com/state/alaska/) - [Alabama](https://isitonrecall.com/state/alabama/) - [Arkansas](https://isitonrecall.com/state/arkansas/) - [Arizona](https://isitonrecall.com/state/arizona/) - [California](https://isitonrecall.com/state/california/) - [Colorado](https://isitonrecall.com/state/colorado/) - [Connecticut](https://isitonrecall.com/state/connecticut/) - [Delaware](https://isitonrecall.com/state/delaware/) - [Florida](https://isitonrecall.com/state/florida/) - [Georgia](https://isitonrecall.com/state/georgia/) - [Hawaii](https://isitonrecall.com/state/hawaii/) - [Iowa](https://isitonrecall.com/state/iowa/) - [Idaho](https://isitonrecall.com/state/idaho/) - [Illinois](https://isitonrecall.com/state/illinois/) - [Indiana](https://isitonrecall.com/state/indiana/) - [Kansas](https://isitonrecall.com/state/kansas/) - [Kentucky](https://isitonrecall.com/state/kentucky/) - [Louisiana](https://isitonrecall.com/state/louisiana/) - [Massachusetts](https://isitonrecall.com/state/massachusetts/) - [Maryland](https://isitonrecall.com/state/maryland/) - [Maine](https://isitonrecall.com/state/maine/) - [Michigan](https://isitonrecall.com/state/michigan/) - [Minnesota](https://isitonrecall.com/state/minnesota/) - [Missouri](https://isitonrecall.com/state/missouri/) - [Mississippi](https://isitonrecall.com/state/mississippi/) - [Montana](https://isitonrecall.com/state/montana/) - [North Carolina](https://isitonrecall.com/state/north-carolina/) - [North Dakota](https://isitonrecall.com/state/north-dakota/) - [Nebraska](https://isitonrecall.com/state/nebraska/) - [New Hampshire](https://isitonrecall.com/state/new-hampshire/) - [New Jersey](https://isitonrecall.com/state/new-jersey/) - [New Mexico](https://isitonrecall.com/state/new-mexico/) - [Nevada](https://isitonrecall.com/state/nevada/) - [New York](https://isitonrecall.com/state/new-york/) - [Ohio](https://isitonrecall.com/state/ohio/) - [Oklahoma](https://isitonrecall.com/state/oklahoma/) - [Oregon](https://isitonrecall.com/state/oregon/) - [Pennsylvania](https://isitonrecall.com/state/pennsylvania/) - [Rhode Island](https://isitonrecall.com/state/rhode-island/) - [South Carolina](https://isitonrecall.com/state/south-carolina/) - [South Dakota](https://isitonrecall.com/state/south-dakota/) - [Tennessee](https://isitonrecall.com/state/tennessee/) - [Texas](https://isitonrecall.com/state/texas/) - [Utah](https://isitonrecall.com/state/utah/) - [Virginia](https://isitonrecall.com/state/virginia/) - [Vermont](https://isitonrecall.com/state/vermont/) - [Washington](https://isitonrecall.com/state/washington/) - [Wisconsin](https://isitonrecall.com/state/wisconsin/) - [West Virginia](https://isitonrecall.com/state/west-virginia/) - [Wyoming](https://isitonrecall.com/state/wyoming/) ## Dates in the source - **Report date**: Jun 10, 2026 - **Recall initiation date**: Apr 20, 2026 - **Center classification date**: Jun 2, 2026 FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable. ## What to do next Read the official notice for the action that applies to your exact product. [Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2294-2026%22) ## Related records [Medical devices records](https://isitonrecall.com/category/medical-devices/) [Shimadzu Medical Systems records](https://isitonrecall.com/brand/shimadzu-medical-systems/)