Philips Intera IT MRI Systems Recalled for Falling Ceiling Speaker Risk
Philips is recalling 11,226 Intera IT MRI systems because ceiling speakers may fall and be pulled by the magnetic field.
What this means for you
Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: The recall involves a structural defect in a medical device where falling components could cause significant injury or property damage, meeting the criteria for a Severe rating.
Plain-English summary
Philips Medical Systems Nederlands is recalling 11,226 Intera IT, Model Number 781160, Nuclear Magnetic Resonance Imaging (MRI) systems. The recall covers all systems distributed nationwide in the United States.
The recall is issued because there is a potential for the ceiling speaker(s) to fall from their position and be pulled to the MR system by the magnetic field. This hazard could result in injury or property damage if the speakers detach and are attracted to the magnet.
Healthcare facilities and consumers with these specific MRI systems should contact Philips Medical Systems Nederlands for instructions on how to resolve the issue. Do not use the affected ceiling speakers until the manufacturer provides guidance.
The recalled product
- Product
- Intera IT, Model Number 781160. Nuclear Magnetic Resonance Imaging System
- Manufacturer
- Philips Medical Systems Nederlands
- Category
- Medical Device — MRI System
- Affected units
- 11,226
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 (1)
- All systems
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 64 recalled by Philips Medical Systems Nederlands under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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