Philips Achieva 7.0T MRI System Recalled for Falling Speaker Hazard
Philips is recalling 11,226 Achieva 7.0T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.
What this means for you
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: The recall involves a risk-of-harm product (falling object due to magnetic field) where injury has not yet been reported, fitting the 'High' severity criteria for theoretical or unreported injury hazards.
Plain-English summary
Philips Medical Systems Nederlands is recalling 11,226 Achieva 7.0T Nuclear Magnetic Resonance Imaging Systems, Model Number 781240. The recall covers all systems distributed nationwide in the United States.
The recall is due to a potential safety hazard where ceiling speakers may fall from their position and be pulled toward the MRI system by the magnetic field. This presents a risk of injury to patients or staff in the vicinity of the equipment.
Healthcare facilities using these systems should contact Philips Medical Systems Nederlands for instructions on how to resolve the issue. The source text does not specify a deadline or specific corrective action steps beyond the recall notification.
The recalled product
- Product
- Achieva 7.0T, Model Number 781240. Nuclear Magnetic Resonance Imaging System
- Manufacturer
- Philips Medical Systems Nederlands
- 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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