Siemens Medical Solutions USA, Inc recalls
Every recall we track for Siemens Medical Solutions USA, Inc — 428 in all, from 2017–2026 — plus the complaints and injury reports the public filed about them. 25 are rated “stop using now”.
Recalls per year, by danger level
Recalls from Siemens Medical Solutions USA, Inc peaked in 2019 (94); 428 since 2017. 6% rated “stop using now”.
All FDA recall records for Siemens Medical Solutions USA, Inc since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 6 | 15 | 0 | 21 |
| 2018 | 0 | 35 | 41 | 1 | 77 |
| 2019 | 11 | 36 | 43 | 4 | 94 |
| 2020 | 3 | 27 | 19 | 0 | 49 |
| 2021 | 0 | 12 | 34 | 0 | 46 |
| 2022 | 1 | 37 | 19 | 0 | 57 |
| 2023 | 0 | 10 | 7 | 1 | 18 |
| 2024 | 8 | 6 | 10 | 0 | 24 |
| 2025 | 2 | 16 | 12 | 4 | 34 |
| 2026 (to date) | 0 | 1 | 7 | 0 | 8 |
Most common reasons for Siemens Medical Solutions USA, Inc recalls
What to do if you have a recalled Siemens Medical Solutions USA, Inc product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Siemens Medical Solutions USA, Inc recalls
60 shown- Use cautionMedical device
Siemens Medical Solutions USA, Inc recalls ARTIS icono ceiling. Model Number: 11328100.
Siemens recalls ARTIS icono ceiling monitors (model 11328100) due to screws loosening over time, potentially causing the monitor to fall. Affected units may need repair or replacement.
SiemensJun 8, 2026 - Lower riskMedical device
Siemens Medical Solutions USA, Inc recalls ARTIS icono floor. Model Number: 11327700.
Siemens recalls ARTIS icono floor model 11327700 due to potential loss of movement capability after adjusting detector lift height to max or min limits. Affected units have specific serial numbers.
SiemensMay 20, 2026 - Lower riskMedical device
Siemens Medical Solutions USA, Inc recalls ARTIS Pheno VE30A and VE40A, Model 10849000
Siemens recalls ARTIS Pheno VE30A and VE40A models 10849000 for potential inaccurate 3D imaging that could lead to unintended low-dose radiation exposure during scans.
SiemensMar 12, 2026 - Lower riskMedical device
Siemens Medical Solutions USA, Inc recalls ARTIS pheno and ARTIS Icono biplane, floor and ceiling. Model Numbers 10849000, 11327600, 11328100, 11327700.
Siemens recalls ARTIS pheno and Icono biplane x-ray systems for potential sporadic dose increases during patient exams. Actual doses remain within regulatory limits but may cause unnecessary radiation exposure.
SiemensMar 10, 2026 - Lower riskMedical device
Siemens Medical Solutions USA, Inc recalls ARTIS Icono biplane, floor and ceiling.: ARTIS icono biplane Model 11327600. ARTIS icono ceiling Model 11328100. ARTIS
Siemens recalls ARTIS Icono biplane and ceiling models that may display 0 x-ray dose during patient exams, but actual radiation is still applied. Affected units have specific model numbers and UDI codes.
SiemensMar 9, 2026 - Lower riskMedical device
Siemens Medical Solutions USA, Inc recalls Interventional Fluoroscopic X-Ray System: LUMINOS Q.namix R; Siemens Material Number (SMN): 11574002; With Software
Siemens recalls specific LUMINOS Q.namix R X-ray systems with software version VB10D-SP02 due to potential display of previous patient images during single image acquisition. Affected units have unique serial numbers listed in the recall notice.
SiemensDec 29, 2025 - Use cautionMedical device
Siemens Medical Solutions USA, Inc recalls NAEOTOM Alpha.Pro Software applications: syngo.CT Brain Quantification syngo.CT Vessel Hyperdensities syngo.CT ASPECTS
Siemens Medical Solutions recalls unapproved CT software applications that lack FDA 510(k) clearance. Affected users should stop using these applications until a fix is available.
SiemensDec 19, 2025 - Lower riskMedical device
Siemens Medical Solutions USA, Inc recalls LUMINOS Lotus Max, Model 11574100 and Luminos dRF Max, Model 10762471
Siemens recalls two ultrasound systems due to potential incorrect collimation when switching between organ programs. Affected models include LUMINOS Lotus Max (11574100) and Luminos dRF Max (10762471).
SiemensDec 5, 2025 - Use cautionMedical device
Siemens Medical Solutions USA, Inc recalls MAMMOMAT Inspiration;
Siemens recalls MAMMOMAT Inspiration models sold with bus-installation kits. These operator tables are designed for stationary use only and not safe for bus installations.
SiemensOct 24, 2025 - UnratedMedical device
Siemens Medical Solutions USA, Inc recalls MAGNETOM Cima.X Upgrade. Model Number: 11689304.
Siemens recalls MAGNETOM Cima.X Upgrade model 11689304 due to potential ice blockage in helium venting system, risking helium leaks in MRI rooms.
SiemensOct 1, 2025 - Use cautionMedical device
Siemens Medical Solutions USA, Inc recalls MAGNETOM Skyra (DE). Model Number: 10432915. 510(k) Numbers: K101347, K111242, K123510, K133435, K140253, K141977,
Siemens recalls MAGNETOM Skyra MRI systems with model 10432915 due to potential ice blockage in helium venting system that could cause pressure build-up and helium leaks during quench events.
SiemensAug 28, 2025 - Lower riskMedical device
Siemens Medical Solutions USA, Inc recalls Artis Pheno. Image-Intensified Flouroscopic X-Ray System.
Siemens recalls Artis Pheno X-ray systems with model 10849000 due to limited movements after startup. Affected units have specific serial numbers. Contact Siemens for details.
SiemensAug 12, 2025 - Stop using nowMedical device
Siemens Medical Solutions USA, Inc recalls UROSKOP Omnia Max. Model Number: 10762473
Siemens Medical recalls UROSKOP Omnia Max models with specific serial numbers due to resistor overheating that could ignite plastic housing. Affected units may need replacement.
Siemens MedicalJun 4, 2025 - Lower riskMedical device
Siemens Medical Solutions USA, Inc recalls interventional fluoroscopic x-ray system
Siemens Medical Solutions recalls interventional fluoroscopic x-ray systems that may incorrectly report high radiation doses due to rare sensor-software communication failure.
SiemensMay 15, 2025 - Lower riskMedical device
SIEMENS MEDICAL SOLUTIONS USA, INC recalls ARTIS One Angiographic X-Ray System
Siemens recalls ARTIS One Angiographic X-Ray Systems due to rare risk of higher radiation dose from incorrect copper prefiltration during x-ray releases. Affected units may require correction to prevent unintended radiation exposure.
SiemensJan 2, 2025 - Lower riskMedical device
Siemens Medical Solutions USA, Inc. recalls ACUSON Juniper 1.0, 1.5, 2.0, 2.5 Diagnostic Ultrasound Systems, REF: 11335791, with software. ACUSON Juniper Select
Siemens recalls ACUSON Juniper 1.0-2.5 ultrasound systems with specific software versions due to potential misdiagnosis from incorrect unit conversions. Affected units may show values 10x smaller than actual liters.
SiemensAug 15, 2024 - Lower riskMedical device
Siemens Medical Solutions USA, Inc recalls Sensis Vibe systems with software version VD15B in combination with Sensis High End Server -Intended to be used as a
Siemens recalls Sensis Vibe systems with VD15B software that may crash when adding certain reporting events. Affected units have specific serial numbers and model numbers. No action is required but users should update software.
Siemens Medical SolutionsJul 3, 2024 - Use cautionMedical device
Siemens Medical Solutions USA, Inc recalls LUMINOS Lotus Max -Intended to visualize anatomical structures by converting an x-ray pattern into a visible image
Siemens recalls LUMINOS Lotus Max X-ray displays due to risk of injury if support arm lowers unexpectedly while positioning near ceiling/wall suspension.
SiemensJul 2, 2024 - Stop using nowMedical device
Siemens Medical Solutions USA, Inc recalls AXIOM Vertix MD - The Vertix MD Trauma has been specially designed for examining emergency and accident patients as
Siemens recalls AXIOM Vertix MD trauma devices due to fire risk from power supply short circuits. Affected units have specific serial numbers and require immediate action to prevent overheating.
SiemensMay 31, 2024 - Use cautionMedical device
Siemens Medical Solutions USA, Inc recalls Siemens Artis Models: Interventional Fluoroscopic X-Ray Systems-Models: Artis zee floor- 10094135 Artis zee ceiling-
Siemens recalls Artis zee and Q series fluoroscopy systems due to potential coolant failure causing system shutdowns and treatment delays. Affected models include Artis zee floor, ceiling, biplane, and Q series units with specific serial numbers.
SiemensMar 21, 2024 - Lower riskMedical device
Siemens Medical Solutions USA, Inc. recalls ACUSON Redwood 1.0 Diagnostic Ultrasound System, REF: 11503314, running software version VA10A to VA10G
Siemens recalls ACUSON Redwood 1.0 ultrasound systems with software VA10A to VA10G due to potential misdiagnosis from incorrect cardiac measurement display. Affected units have specific serial numbers listed in the recall.
SiemensFeb 23, 2024 - Lower riskMedical device
Siemens Medical Solutions USA, Inc recalls Sensis Vibe Hemo
Siemens recalls Sensis Vibe Hemo devices with specific serial numbers due to potential documentation crashes. Affected units may experience application failures; contact for remedy.
SiemensNov 29, 2023 - Use cautionMedical device
Siemens Medical Solutions USA, Inc recalls ARTIS icono (ceiling configuration), Fluoroscopic x-ray system; Model no. 11328100
Siemens recalls ARTIS icono ceiling x-ray systems with model 11328100 due to false collision signals after power off, risking temporary system unavailability during procedures.
SiemensOct 17, 2023 - Use cautionMedical device
Siemens Medical Solutions USA, Inc recalls Mobilett Mira wireless (VA20) mobile x-ray system(s)
Siemens recalls Mobilett Mira wireless (VA2:0) mobile x-ray systems due to no acoustic signal during x-ray activation. The system functions correctly but requires visual confirmation of x-ray release.
SiemensOct 5, 2023 - Use cautionMedical device
Siemens Medical Solutions USA, Inc recalls ***Updated 12/4/23*** (1) Cios Flow (VA30) mobile fluoroscopic C-arm X-ray System. Designed for the surgical
Siemens recalls Cios Flow mobile X-ray systems with software issue that may lead to patient misdiagnosis or repeat imaging. Affected units have specific serial numbers and material numbers.
SiemensSep 12, 2023 - Lower riskMedical device
Siemens Medical Solutions USA, Inc recalls (1) Over-ear headphones used with the MAGNETOM Amira MAGNETOM Free.Star MAGNETOM Sempra, MAGNETOM Free.Max, MAGNETOM
Siemens recalls over-ear headphones used with specific MRI systems due to lubricating grease causing visible artifacts during head scans. Affected models include MAGNETOM Amira, Free.Max, Free.Star, Sempra, Mica, Spectra and others.
SiemensSep 1, 2023 - Lower riskMedical device
Siemens Medical Solutions USA, Inc. recalls ACUSON Redwood 2.0 ultrasound systems, REF: 11503314
Siemens recalls ACUSON Redwood 2.0 ultrasound systems with software version VA20. Using an 18L6 transducer from a 1.0 system with a 2.0 system may cause underestimated measurements in Dual view, risking misdiagnosis.
SiemensJul 13, 2023 - Lower riskMedical device
Siemens Medical Solutions USA, Inc. recalls The following Pro.specta Emission Computed Tomography Systems that were manufactured with an SLD Look Ahead Optical
Siemens recalls specific Pro.specta Emission Computed Tomography Systems with SLD Look Ahead Optical Sensor Assembly that may cause reduced image resolution during scans. Affected models and serial numbers listed in the recall notice.
SiemensJul 12, 2023 - Use cautionMedical device
Siemens Medical Solutions USA, Inc recalls ARTIS pheno-Angiography systems developed for single and biplane diagnostic imaging and interventional procedures.
Siemens recalls ARTIS pheno-Angiography systems with specific serial numbers due to potential thermal overload in cable connectors during excessive fluoroscopy, risking imaging loss and treatment delays.
SiemensJun 19, 2023 - Use cautionMedical device
Siemens Medical Solutions USA, Inc recalls Cios Select VA 21 with FD- A Mobile X-ray system intended for use in Operating room, Traumatology, Endoscopy, Intensive
Siemens recalls Cios Select VA 21 mobile X-ray systems due to potential electric shock from liquid ingress if plexiglass cover falls off. Affected units have specific serial numbers and were sold for medical use. Contact Siemens for details.
SiemensJun 5, 2023 - Lower riskMedical device
Siemens Medical Solutions USA, Inc recalls ARTIS one with a hybrid cable- An angiography system developed for diagnostic imaging and interventional procedures.
Siemens recalls ARTIS One angiography systems with hybrid cables that may have no image display. Affected units have specific serial numbers; contact for remedy.
SiemensMar 21, 2023 - Use cautionMedical device
Siemens Medical Solutions USA, Inc recalls ARTIS pheno systems with a Siemens Healthineers table or Trumpf/MAQUET table (OEM)- Angiography systems developed for
Siemens recalls ARTIS pheno angiography systems with specific table models due to potential 5-10mm C-arm positioning error during procedures, risking patient or staff injury.
SiemensFeb 2, 2023 - Use cautionMedical device
Siemens Medical Solutions USA, Inc recalls ARTIS pheno systems with a Siemens Healthineers table or a Trumpf/ MAQUET table-A Fluoroscopic X-Ray system. Material #
Siemens Healthineers recalls ARTIS pheno systems with specific Siemens Healthineers or Trumpf/MAQUET tables due to risk of patient or staff injury from unintended table movement.
Siemens HealthineersFeb 2, 2023 - Lower riskMedical device
Siemens Medical Solutions USA, Inc. recalls SIEMENS Biograph mCT: a) Flow 64-4R Seismic, b) S(40)-3R Seismic, c) S(64)-3R Seismic, d) S(40)-4R Seismic, e) S(64)-4R
Siemens recalls specific Biograph mCT models due to potential gantry locking mechanism failure. Affected units may not secure properly during scanning or service, risking equipment damage or safety issues.
SiemensJan 16, 2023 - Lower riskMedical device
Siemens Medical Solutions USA, Inc recalls Software : myNeedle Guide 2D license, myNeedle Guide 2D AWP only Workflow license, or myNeedle Guide 3D license. Used
Siemens recalls specific myNeedle Guide software licenses for CT systems due to swapped orientation labels in axial slices, which may cause misalignment during procedures. Affected models include SOMATOM go.Now, go.Up, go.All, and others with listed serial numbers and UDI codes.
SiemensDec 22, 2022 - Use cautionMedical device
Siemens Medical Solutions USA, Inc recalls Luminos dRF Max with software VE10, VF10, VF11- A diagnostic imaging system for radiographic and fluoroscopic studie
Siemens recalls Luminos dRF Max imaging systems with software VE10, VF10, VF11 due to room configuration risks that could cause serious injury from collisions with walls or ceilings.
SiemensDec 21, 2022 - Use cautionMedical device
Siemens Medical Solutions USA, Inc recalls System Material # Artis zee floor 10094135 Artis zee ceiling 10094137 Artis zee multi-purpose 10094139 Artis zee
Siemens recalls Artis zee floor, ceiling, and multi-purpose X-ray systems that may only boot into backup mode after abrupt shutdowns, requiring treatment cancellation or alternative systems.
SiemensDec 16, 2022 - Use cautionMedical device
Siemens Medical Solutions USA, Inc recalls ARTIS pheno, ARTIS icono biplane, and ARTIS icono floor
Siemens Medical recalls ARTIS pheno, icono biplane, and icono floor models due to risk of tabletop detachment. Affected units have specific material and UDI/DI numbers. Contact for repair or replacement.
Siemens MedicalDec 16, 2022 - Use cautionMedical device
Siemens Medical Solutions USA, Inc recalls Luminos Agile Max, Luminos dRF Max, and LUMINOS Lotus Max
Siemens recalls Luminos Agile Max, dRF Max, and Lotus Max models due to potential footrest detachment during use, which could cause injury. Affected units have specific serial numbers and are used in medical imaging.
SiemensDec 9, 2022 - Lower riskMedical device
Siemens Medical Solutions USA, Inc recalls Luminos Agile Max (VE10, VF10, VF11)
Siemens recalls Luminos Agile Max (VE10, VF10, VF1:1) fluoroscopy systems that may display incorrect air kerma rates during exams. No impact on diagnosis or workflow, but potential for rare errors in specific systems.
SiemensNov 23, 2022 - Lower riskMedical device
Siemens Medical Solutions USA, Inc recalls Programmable Diagnostic Computer
Siemens recalls programmable diagnostic computers with software version VD12A due to potential procedure delays from software errors. Owners should check model numbers and contact Siemens for updates.
SiemensNov 16, 2022 - Use cautionMedical device
Siemens Medical Solutions USA, Inc recalls ARTISTE, ONCOR and PRIMUS with syngo RT Therapist with software version 4.3.1 MR3. Material Number: 8162815 Intended
Siemens recalls ARTISTE, ONCOR and PRIMUS radiation therapy systems with software version 4.3.1 MR3 due to risk of delivering radiation to the wrong body site during cancer treatment. Affected units have specific serial numbers and material numbers.
SiemensNov 9, 2022 - Use cautionMedical device
Siemens Medical Solutions USA, Inc recalls ARTIS pheno, Interventional fluoroscopic x-ray system, Model No. 10849000
Siemens recalls ARTIS pheno interventional fluoroscopy systems with software version VE10B due to potential treatment delays. Affected units may require switching to another system if procedures cannot continue.
SiemensSep 20, 2022 - Use cautionMedical device
Siemens Medical Solutions USA, Inc recalls Artis icono biplane- Model No. 11327600 Artis icono floor- Model No. 11327700
Siemens recalls Artis Icono biplane and floor models with specific serial numbers due to rare risk of X-ray system shutdown if error detection fails. Affected units may require repair.
SiemensAug 10, 2022 - Use cautionMedical device
Siemens Medical Solutions USA, Inc recalls AXIOM Sensis or Sensis Vibe Combo systems as follows: System Material # AXIOM Sensis, Combo 64 6623974; AXIOM Sensis,
Siemens recalls Sensis Combo systems with specific serial numbers due to potential patient touch leakage current and liquid spillage risks. Affected units include AXIOM Sensis models with serial numbers listed in the recall notice.
SiemensJul 12, 2022 - Lower riskMedical device
Siemens Medical Solutions USA, Inc recalls Sensis with software version VD12A. A diagnostic and administrative tool supporting hemodynamic catheterizations and/or
Siemens recalls Sensis software version VD12A for potential disconnect during first patient exam or after inactivity, risking no vital signs. Affected units have specific serial numbers and model.
SiemensJun 15, 2022 - Lower riskMedical device
Siemens Medical Solutions USA, Inc recalls Artis Pheno, Interventional Fluoroscopic X-Ray System, Model No. 10849000
Siemens recalls Artis Pheno Interventional Fluoroscopy Systems with model 10849000 due to rare video signal loss in displays, potentially causing image loss during procedures. Affected units include specific serial numbers listed in the recall.
SiemensJun 10, 2022 - Use cautionMedical device
Siemens Medical Solutions USA, Inc recalls Artis zeego (Model no. 10280959) and Artis Q.zeego (Model no. 10848283), Interventional Fluoroscopic X-Ray System
Siemens recalls Artis zeego and Artis Q.zeego X-ray systems with model numbers 10280959 and 10848283 due to potential stand movement failure after BIOS battery discharge during startup.
SiemensMay 24, 2022 - Lower riskMedical device
Siemens Medical Solutions USA, Inc recalls Artis Icono, Interventional Fluoroscopic X-Ray System, Model No. 11327600
Siemens recalls Artis Icono X-Ray System model 11327600 due to potential electrical failure from increased fan wear during system tests, which could cause image system malfunction.
SiemensMay 20, 2022 - Use cautionMedical device
Siemens Medical Solutions USA, Inc recalls Sensis, Programmable Diagnostic Computer, Model Nos. 6623974 6634633 6634658 6648153 6648161 10140973 10764561 10765502
Siemens recalls Sensis programmable diagnostic computers with specific model numbers due to potential software issues that may cause treatment interruptions for patients.
Siemens Medical SolutionsApr 13, 2022 - Use cautionMedical device
Siemens Medical Solutions USA, Inc recalls Artis icono biplane -angiography systems developed for single and biplane diagnostic imaging and interventional
Siemens recalls Artis Icono Biplane angiography systems due to potential electric shock if protective earth is interrupted and a fault current occurs. Affected units have specific serial numbers.
SiemensApr 11, 2022 - Use cautionMedical device
Siemens Medical Solutions USA, Inc. recalls Symbia Intevo Bold and Symbia Intevo 6 SPECT/CT Systems
Siemens recalls Symbia Intevo Bold and Symbia Intevo 6 SPECT/CT systems due to potential safety risks from faulty bolts holding CT balancing weights.
SiemensMar 11, 2022 - Lower riskMedical device
Siemens Medical Solutions USA, Inc recalls YSIO X.Pree
Siemens recalls YS: X.Pree x-ray machines due to incorrect collimation display on user interface, potentially causing improper x-ray coverage. Affected units sold in the US with model 11107464.
Siemens Medical SolutionsMar 7, 2022 - Lower riskMedical device
Siemens Medical Solutions USA, Inc recalls syngo.via RT Image Suite upgraded to VB60 running on SOMATOM go.Up Model Number 11061620. Running on servers with
Siemens recalls syngo.via RT Image Suite software version VB60 for SOMATOM go.Up scanners. Upgraded software may display incorrect laser coordinates during patient marking, risking misalignment. Affected units have specific model numbers and serials.
SiemensMar 7, 2022 - Lower riskMedical device
Siemens Medical Solutions USA, Inc recalls SIEMENS SOMATOM with software syngo CT VA30A_SP4 Models: SOMATOM go.Now 11061610 & 11061618 SOMATOM go.Up 11061620 &
Siemens recalls certain SOMATOM CT scanners with software syngo CT VA30A_SP4 that may cause scanning workflow interruptions, unexpected notifications, and image artifacts. Affected models include SOMATOM go.Now, go.Up, go.All, go.Top, go.Sim, go.Open Pro, and X.cite.
SiemensMar 7, 2022 - Use cautionMedical device
Siemens Medical Solutions USA, Inc. recalls Acuson 9vE4 Transducer, Model (240)11289564 CE0129, Rx Only ,
Siemens recalls specific Acuson 9vE4 ultrasound transducers that may overheat, risking damage to equipment and potential injury. Affected units have unique serial numbers listed in the recall notice.
SiemensMar 7, 2022 - Use cautionMedical device
Siemens Medical Solutions USA, Inc recalls syngo Application software VE20 (Material Number 10848815) installed on the Artis pheno and Artis icono systems as
Siemens recalls Artis pheno and icono CT systems with syngo VE20 software (Material 10848815) due to potential patient misorientation after Toshiba CT data loading. Affected units may require software update.
SiemensFeb 25, 2022 - Lower riskMedical device
Siemens Medical Solutions USA, Inc recalls Artis icono floor in combination with a Siemens Healthineers table or Trumpf/MAQUET table (OEM). Intended use single
Siemens recalls Artis Icono floor systems with certain Siemens Healthineers or Trumpf/MAQUET tables due to potential software errors that may delay clinical treatment. Affected units have specific serial numbers and model codes.
SiemensFeb 25, 2022 - Use cautionMedical device
Siemens Medical Solutions USA, Inc recalls Artis zee floor MN, Model Number 10094142
Siemens recalls Artis zee floor MN model 10094142 due to risk of X-ray tube overheating if coolant level drops. Affected units may display error messages and block X-ray use.
SiemensFeb 23, 2022 - Use cautionMedical device
Siemens Medical Solutions USA, Inc recalls Ysiosystem with VC10 software version, Model Number 10281013. Radiographic system
Siemens recalls Ysio radiographic systems with VC10 software version 10281013 due to a software error that may cause unintended tube stand movement, creating collision risk for people or objects.
SiemensJan 31, 2022
Siemens Medical Solutions USA, Inc recall questions
How many recalls has Siemens Medical Solutions USA, Inc had?
428 recalls from Siemens Medical Solutions USA, Inc are on record with U.S. safety agencies, from 2017–2026.
What is the most recent Siemens Medical Solutions USA, Inc recall?
Siemens Medical Solutions USA, Inc recalls ARTIS icono ceiling. Model Number: 11328100., dated Jun 8, 2026. Every Siemens Medical Solutions USA, Inc recall is listed on this page, newest first.
Why are Siemens Medical Solutions USA, Inc products recalled?
The most common reasons on record: A potential risk of unnecessary radiation exposure due to a software issue (7); Potential for liquid entry (3); DAP chamber may be missing an insulating foil (2); There is potential for the footrest to detach from the patient table during use. (2).
What should I do if I have a recalled Siemens Medical Solutions USA, Inc product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Siemens Medical Solutions USA, Inc recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.