Philips AlIura Xper F010 F Monitor Ceiling Suspension Recall
Philips is recalling AlIura Xper F010 F systems because the monitor ceiling suspension may detach, causing the monitor to fall and potentially injure patients, users, or bystanders.
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 where the monitor may fall and cause injury, but the source text does not report any actual injuries or illnesses, fitting the 'High' severity criteria for theoretical or unreported harm.
Plain-English summary
Philips Electronics North America Corporation is recalling 5,115 AlIura Xper F010 F systems, System Code 722002. These systems are used for vascular, cardiovascular, and neurovascular imaging, cardiac imaging diagnostics, and non-vascular interventions.
The recall is due to a potential defect in the Monitor Ceiling Suspension, which holds a large screen monitor. The suspension may detach from the actuator rotor shaft, causing the monitor to fall. If this occurs, there is a risk of injury to the patient, user, and bystanders.
The affected units are all systems with an actuator for the FlexVision Monitor Ceiling Suspension manufactured between 2003 and May 2011. These systems were distributed nationwide in the United States and in numerous countries worldwide. Consumers and healthcare facilities should contact Philips for instructions on how to address this safety issue.
The recalled product
- Product
- AlIura Xper F010 F, System Code 722002 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging applications including diagnostics, Non-vascular interventions
- Manufacturer
- Philips Electronics North America Corporation
- Affected units
- 5,115
Distribution
Part of a larger recall action
This product is one of 27 recalled by Philips Electronics North America Corporation 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.
See all 27 products in this recall →Related recalls
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