Manufacturer
796 recalls in our database name Siemens Medical Solutions USA, Inc. as the manufacturing or recalling firm.
Of the 796 recalls from Siemens Medical Solutions USA, Inc. we have scored against our rubric, 16 (2%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 69 (9%) are Severe.
The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.
Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.
Siemens Medical Solutions is recalling SOMATOM Spirit CT scanners due to a software issue that may cause unnecessary radiation exposure.
Siemens Medical Solutions is recalling SOMATOM Emotion 16 CT scanners due to a software issue that may cause unnecessary radiation exposure.
Siemens is recalling SOMATOM Scope Power units due to a software issue that may cause unnecessary radiation exposure.
Siemens Medical Solutions is recalling SOMATOM Perspective CT scanners due to a software issue that may cause unnecessary radiation exposure.
Siemens Medical Solutions is recalling SOMATOM Emotion 6 CT scanners due to a software issue that may cause unnecessary radiation exposure.
Siemens Medical Solutions is recalling SOMATOM Scope devices due to a software issue that may cause unnecessary radiation exposure.
Siemens Medical Solutions USA is recalling SOMATOM Perspective 16 CT scanners due to a software issue that may cause unnecessary radiation exposure.
Siemens is recalling Artis zee angiography systems with specific Laird cooling units due to defective seals that may allow coolant to leak into electrical parts, potentially causing sudden system shutdowns.
Siemens is recalling six AXIOM Artis angiography systems in the US due to a defective sealing that could allow coolant to leak into electrical parts.
Siemens is recalling 40 ARTIS Pheno Fluoroscopic X-Ray systems because the C-arm can drop up to 40 mm during specific high-speed rotations.
Siemens is recalling 68 Artis zee biplane systems because the large display may remain black after exiting power save mode, potentially requiring treatment cancellation or patient transfer.
Siemens Medical Solutions is recalling two Artis Q.zen biplane systems because the display may fail to show images after power save mode, potentially requiring treatment cancellation or patient transfer.
Siemens is recalling 73 Artis zee ceiling units because the display may fail to show images after power save mode, potentially requiring procedure cancellation.
Siemens is recalling Artis zee floor MN systems because the display may fail to show images after power save mode, potentially requiring procedure cancellation.
Siemens is recalling Artis zee MP systems because the display may fail to show an image after power save mode, potentially requiring procedure cancellation or patient transfer.
Siemens is recalling 39 ARTIS Pheno Interventional Fluoroscopic X-Ray Systems because the C-arm may drop up to 20 mm, potentially injuring patients.
Siemens Medical Solutions is recalling 56 Artis zeego systems because the display may fail to show images after power save mode, potentially requiring procedure cancellation.
Siemens is recalling Artis Q.zen floor units because the display may fail to show images after power save mode, potentially requiring procedure cancellation or patient transfer.
Siemens is recalling five Artis Q biplanes because the display may fail to show an image after power save mode, potentially requiring procedure cancellation or patient transfer.
Siemens Medical Solutions is recalling five Artis Q ceiling units because the display may fail to show an image after exiting power save mode, potentially requiring treatment cancellation.
Siemens is recalling 14 Artis zee floor systems because the display may fail to show images after power save mode, potentially requiring treatment cancellation.
Siemens is recalling four Artis Q.zeego X-ray systems because the display may remain black after power save mode, preventing normal operation and requiring procedure cancellation or patient transfer.
Siemens is recalling two Artis zee biplane MN systems because the large display may fail to show an image after power save mode, potentially requiring procedure cancellation or patient transfer.
Siemens Medical Solutions is recalling 405 Biograph mCT systems because laser cover windows may fall off, posing a potential hazard.
Siemens is recalling 33 SOMATOM Go.Up CT scanners in the US due to a potential software issue that may require patient rescans.