Upgrade to MR 7700 Model Number (REF): 782130;
Pending LLM rewrite. Source: FDA_DEVICE Z-2218-2025.
Severity not yet assessed
We have not scored this recall against our rubric yet, so we are not showing a severity rating or our usual guidance. The agency’s own notice below is the authoritative source — read it first.
Plain-English summary
The potential for component failures in the Gradient Coil of the affected MR systems may act as a heat source with a potential to produce smoke and/or fire.
The recalled product
- Product
- Upgrade to MR 7700 Model Number (REF): 782130;
- Manufacturer
- Philips North America
- Category
- Medical Device — Devices
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (20)
- Model Number (REF): 782130
- UDI-DI: 00884838104402
- Serial Numbers: 42030
- 42037
- 42066
- 42151
- 42163
- 42164
- 42211
- 42219
- 42248
- 42376
- 45001
- 45007
- 45051
- 45052
- 45179
- 45236
- 45297
- 45298
Distribution
Distributed nationwide across the United States.
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