Philips Allura Xper F010/10 DRTable Recall for Monitor Suspension Defect
Philips is recalling 5,115 Allura Xper F010/10 DRTables 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 injury has not yet been reported, fitting the High severity criteria for potential physical injury from falling equipment.
Plain-English summary
Philips Electronics North America Corporation is recalling 5,115 Allura Xper F010/10 DRTables (System Code 722019) used for vascular, cardiovascular, neurovascular, and cardiac imaging applications. The recall affects systems manufactured between 2003 and May 2011 that include an actuator for the FlexVision Monitor Ceiling Suspension.
The recall is due to a potential defect where the Monitor Ceiling Suspension, which holds a large screen monitor, may detach from the actuator rotor shaft. If this occurs, the monitor may fall from the ground, posing a risk of injury to patients, users, and bystanders.
The affected units were distributed nationwide in the United States and in numerous countries worldwide. Healthcare facilities should contact Philips to arrange for the necessary corrective actions to address the suspension defect.
The recalled product
- Product
- Allura Xper F010/10 DRTable, System Code 722019 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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