MAGNETOM AmiraRecalls & reported problems across all models

We found 2 models of MAGNETOM Amira by Siemens Shenzhen Magnetic Resonance Ltd. in the FDA's device registry (GUDID). None of them is named in an adverse event report in our data.

1 FDA recall record name at least one of these models by its device identifier, 1 still open.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works

MAGNETOM Amira recalls

FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.

1. Sep 1, 2023Open, Classified

   In some cases, when lubricating grease is present within the headband of the over-ear headphones, it may cause visible, dot- or lineshaped, fat-isointense artifacts during head examinations only. These potential artifacts depend on the position of the headband, the amount of lubricating grease, as well as the sequence parameters used

   Z-2648-2023 · Root cause: Process control · names 2 of these models · Recall details · FDA record ↗

MAGNETOM Amira models

2 models, most reported first. Each model has its own page with its reports, recalls and device details.

• MAGNETOM Amira 10836777

  System, nuclear magnetic resonance imaging
  1 recall0 reports
• MAGNETOM Amira 10838610

  System, nuclear magnetic resonance imaging
  1 recall0 reports

Other Siemens Shenzhen Magnetic Resonance Ltd. products

• MAGNETOM Sempra2 models · 2 reports · 1 recall
• MAGNETOM Spectra2 models · 2 reports · 1 recall
• MAGNETOM Free.Max2 models · 0 reports · 1 recall