Philips Achieva 3.0T MRI System Recalled for Ceiling Speaker Hazard
Philips is recalling Achieva 3.0T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.
The agency’s classification
FDA (Devices): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 4/5 (Severe).
The hazard poses a serious risk of illness, injury, or structural failure. 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 objects could cause significant injury or property damage, meeting the criteria for a Severe rating.
Plain-English summary
Philips Medical Systems Nederlands is recalling the Achieva 3.0T for PET, Model Number 781477, Nuclear Magnetic Resonance Imaging System. The recall involves 11,226 total units 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 or property damage if the speakers detach and are attracted to the magnet.
Healthcare facilities and users of these MRI systems should contact Philips Medical Systems Nederlands for instructions on how to address the issue. The source text does not specify a deadline or immediate shutdown requirement, but users should follow the manufacturer's guidance to mitigate the risk.
The recalled product
- Product
- Achieva 3.0T for PET, Model Number 781477. 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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