Coil, Magnetic Resonance, Specialty
FDA adverse event reports and recall history for coil, magnetic resonance, specialty (product code MOS), from the public MAUDE corpus and the live FDA recall database.
- Total reports
- 134
- Deaths
- 0
- Injuries
- 82
- Malfunctions
- 26
Reports per year
Source: FDA adverse event reports by year received, 2012–2026. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Recent recalls
- 2024-11-25Open, ClassifiedUse error
Achieva TX Interventional Coil 3.0T
Potential safety issue where a patient may be harmed while preparing for or during a scan.
- 2024-11-25Open, ClassifiedUse error
dS Breast 16ch 1.5T
Potential safety issue where a patient may be harmed while preparing for or during a scan.
- 2024-11-25Open, ClassifiedUse error
dS Breast 16ch 3.0T
Potential safety issue where a patient may be harmed while preparing for or during a scan.
- 2024-11-25Open, ClassifiedUse error
dS Breast 7ch 1.5T
Potential safety issue where a patient may be harmed while preparing for or during a scan.
- 2024-11-25Open, ClassifiedUse error
dS Breast 7ch 3.0T
Potential safety issue where a patient may be harmed while preparing for or during a scan.
- 2024-11-25Open, ClassifiedUse error
Mammotrak Diagnostic Coil 1.5T
Potential safety issue where a patient may be harmed while preparing for or during a scan.
- 2024-11-25Open, ClassifiedUse error
Mammotrak Interventional Coil 1.5T
Potential safety issue where a patient may be harmed while preparing for or during a scan.
- 2024-11-25Open, ClassifiedUse error
Mammotrak Diagnostic Coil 3.0T
Potential safety issue where a patient may be harmed while preparing for or during a scan.
- 2024-11-25Open, ClassifiedUse error
Mammotrak Interventional Coil 3.0T
Potential safety issue where a patient may be harmed while preparing for or during a scan.
- 2024-11-25Open, ClassifiedUse error
SENSE Breast Coil
Potential safety issue where a patient may be harmed while preparing for or during a scan.
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