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Siemens Medical Solutions USA, Inc

Siemens Medical Solutions USA, Inc Recalls

All product recalls associated with Siemens Medical Solutions USA, Inc.

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Recall Summary

Total Recalls

1000

Past Year

Class I (Serious)

Most Recent

Dec 2025

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 801–820 of 1121 recalls

Siemens Medical Solutions USA, Inc: AXIOM Sireskop SD Model numbers 8890415 and 8890407. The...

During interventional use and applications, the possibility exists for liquids to enter the systems.

FDAJan 8, 2009Nationwide• Siemens Medical Solutions USA, Inc

Siemens Medical Solutions Diagnostics: Immulite 2000 and Immulite 2500 digital Fluidics PC Board...

Design Flaw: The redesign of the Digital Fluidics PCB used in IMMULITE 2000 and IMMULITE 2500 is missing a jumper.

FDAJan 5, 2009AZ, CA, FL +12 more• Siemens Medical Solutions Diagnostics

Siemens Medical Solutions USA, Inc: Artiste MV Digital Linear Accelerator System Equipped wit...

The range of tolerance is to high for the accessory holder, therefore, Wedges and other accessories do not latch to the locking mechanism correctly.

FDA

1...39 404142 43...57

Page 41 of 57Next

Dec 20, 2008

Nationwide

• Siemens Medical Solutions USA, Inc

Siemens Medical Solutions USA, Inc.: Siemens Medical Solutions E.CAM Patient Handling System (...

Patient fingers can get pinched if they attempt to pull themselves up from the patient handling system without any assistance and grabbing onto the flip-up FOV indicator bars.

FDADec 18, 2008Nationwide• Siemens Medical Solutions USA, Inc.

GE Healthcare Integrated IT Solutions: GE Centricity PACS RA1000 Workstation (for diagnostic ima...

There is a potential patient safety issue involving the use of the F12 keyboard Approve & Complete function. The issue may cause erroneous information to be added to a report when trying to approve and complete it.

FDADec 12, 2008Nationwide• GE Healthcare Integrated IT Solutions

GE Healthcare Integrated IT Solutions: Centricity Enterprise Web 3.0 software; the software allo...

Software error: There are two potential safety situations with Centricity Enterprise Web software - a forced log off may occur while using the Centricity Enterprise Web during an open session, and Centricity Enterprise Web does not utilize calibration performed on image measurements in Centricity RA1000 Workstation.

FDADec 12, 2008Nationwide• GE Healthcare Integrated IT Solutions

Siemens Medical Solutions USA, Inc: Somatom Definition AS, Model number 8098027. Computed to...

possible improper installation of tilt transport lock/tilt limiter

FDADec 9, 2008Nationwide• Siemens Medical Solutions USA, Inc

GE Healthcare Integrated IT Solutions: GE Centricity PACS RA1000 Workstation (for diagnostic ima...

There is a potential patient safety issue involving patient jacket content, which may result in unintended historical image(s) being displayed.

FDANov 21, 2008Nationwide• GE Healthcare Integrated IT Solutions

GE Healthcare Integrated IT Solutions: GE Centricity PACS RA1000 Workstation (for diagnostic ima...

Unread exams may inadvertently get marked as dictated in PACS workstation when the user signs off the report in Talkstation and opens the next exam.

FDANov 20, 2008CA, FL, IL +8 more• GE Healthcare Integrated IT Solutions

GE Healthcare Integrated IT Solutions: Centricity TriWin Laboratory Information System; GE Healt...

A software defect in the Centricity Lab (TriWin) product may incorrectly link patient information to a wrong report. Also, when viewing results in Patient Viewer, and a coagulation result is higher or lower than the linearity limit, then all of the results following the higher or lower result will show the same result as the first flagged result.

FDANov 17, 2008Nationwide• GE Healthcare Integrated IT Solutions

Siemens Medical Solutions USA, Inc: CT syngo Dual Energy Viewer on the syngo Multimodality Wo...

Indicated orientation does not match actual orientation of the patient.

FDANov 13, 2008Nationwide• Siemens Medical Solutions USA, Inc

Siemens Medical Solutions USA, Inc: Drive Belt for Radiation Therapy Simulation systems SIMVI...

Excessive wear on drive belts used for Image Intensifier and/or X-ray head drive mechanisms may result in uncontrolled movement, which may cause injury.

FDANov 6, 2008Nationwide• Siemens Medical Solutions USA, Inc

Siemens Medical Solutions USA, Inc: Artiste MV Digital Linear Accelerator, when used in combi...

Under certain conditions, the flat panel may move unexpectedly and collide with the patient.

FDAOct 23, 2008Nationwide• Siemens Medical Solutions USA, Inc

Siemens Medical Solutions USA, Inc: Artiste MV SA Linear Accelerator with syngo RT Therapist ...

If a plan contains a sequence of beams, including at least 1 ARC treatment beam and if during the setup stage of a beam following an ARC beam in the delivery sequence a termination occurs, and the user selects the immediate resumption feature, syngo RT Therapist Express systems will display and record a second delivery of a prior beam and not the delivery of the current beam in certain circumstanc

FDAOct 23, 2008Nationwide• Siemens Medical Solutions USA, Inc

Siemens Medical Solutions USA, Inc.: Symbia T6 System; a dual-detector variable angle gamma ca...

The protective plastic cap over the CT gantry power switch on the Line Connection Box may come loose, exposing the energized electrical contacts within the switch, thereby causing an electric hazard.

FDASep 29, 2008Nationwide• Siemens Medical Solutions USA, Inc.

Siemens Medical Solutions USA, Inc.: Symbia T16 System; a dual-detector variable angle gamma c...

The protective plastic cap over the CT gantry power switch on the Line Connection Box may come loose, exposing the energized electrical contacts within the switch, thereby causing an electric hazard.

FDASep 29, 2008Nationwide• Siemens Medical Solutions USA, Inc.

GE Healthcare Integrated IT Solutions: GE Centricity PACS RA1000 Workstation (for diagnostic ima...

Software anomalies result in patient safety issues involving patient jacket content intermittently becoming unintentionally out of synchronization with the images being displayed, and involving Default Display Protocols (DDPs) which are used to layout images when displaying a study. If the user does not check the Study Date Time of the exam on the image title bar, then they may interpret the curr

FDASep 25, 2008Nationwide• GE Healthcare Integrated IT Solutions

GE Healthcare Integrated IT Solutions: GE Healthcare Centricity Perinatal (formerly Quantitative...

Software anomalies in the Alert and Reminder feature could result in a delay of treatment. When attempting to select the last visible alert or reminder choice, the next choice on the list below the desired choice is selected, and an inconsistent color may be displayed for the same clinical element across a set of work stations.

FDASep 25, 2008Nationwide• GE Healthcare Integrated IT Solutions

GE Healthcare Integrated IT Solutions: Centricity Perinatal (formerly Quantitative Sentinel) Sys...

On the I&O chart, the IN, OUT and NET fluid totals values will not honor the numeric precision configuration, always displaying a whole number, losing decimal point accuracy.

FDASep 25, 2008Nationwide• GE Healthcare Integrated IT Solutions

GE Healthcare Integrated IT Solutions: GE Centricity Ultra Laboratory System Software; for recor...

Software computer, error: The abnormal result flag is not being sent in the HL7 messages on results that are lower than the normal range. For further information, please telephone GE Healthcare Integrated IT Solutions at 800-437-1171.

FDASep 22, 2008Nationwide• GE Healthcare Integrated IT Solutions