MR CoilsRecalls & reported problems across all models
Philips Medical Systems Nederland B.V. · 3 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
3 open recalls name at least one MR Coils model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls
- 3
We found 3 models of MR Coils by Philips Medical Systems Nederland B.V. in the FDA's device registry (GUDID). None of them is named in an adverse event report in our data.
3 FDA recall records name at least one of these models by its device identifier, 3 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
MR Coils 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.
- Nov 4, 2024Open, Classified
Potential safety issue where a patient may be harmed while preparing for or during a scan.
Z-0540-2025 · Root cause: Use error · Recall details · FDA record ↗
- Nov 4, 2024Open, Classified
Potential safety issue where a patient may be harmed while preparing for or during a scan.
Z-0538-2025 · Root cause: Use error · Recall details · FDA record ↗
- Nov 4, 2024Open, Classified
Potential safety issue where a patient may be harmed while preparing for or during a scan.
Z-0537-2025 · Root cause: Use error · Recall details · FDA record ↗
MR Coils models
3 models, most reported first. Each model has its own page with its reports, recalls and device details.
- MR Coils dS Breast 16ch 3.0TCoil, Magnetic Resonance, Specialty1 recall0 reports
- MR Coils dS Breast 7ch 3.0TCoil, Magnetic Resonance, Specialty1 recall0 reports
- MR Coils dS Breast 16Ch 1.5TCoil, Magnetic Resonance, Specialty1 recall0 reports
Other Philips Medical Systems Nederland B.V. products
- Allura Xper FD19 models · 15,187 reports · 84 recalls
- Azurion22 models · 9,199 reports · 71 recalls
- Ingenia54 models · 479 reports · 138 recalls
- IntelliSpace Cardiovascular11 models · 439 reports · 3 recalls
- MR 7000 Series2 models · 4 reports · 11 recalls
- Dynamic Coronary Roadmap3 models · 10 reports · 9 recalls
- MR 5000 Series3 models · 11 reports · 8 recalls
- Brilliance iCT2 models · 9 reports · 8 recalls
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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