Philips Azurion patient tables recalled for finger entrapment risk
Philips is recalling Azurion 7 M12 and Allura patient tables used in medical imaging systems due to a finger entrapment hazard during manual repositioning. Operators and service personnel may suffer finger injury if fingers are caught between the tabletop and guiding rails.
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: FDA Class II recall for a risk-of-harm medical device where finger entrapment during manual repositioning may result in injury, but no incidents or illnesses have been reported. The hazard is potential rather than confirmed.
Plain-English summary
Philips Medical Systems is recalling specific Azurion 7 M12 patient tables (AD7 and AD7X models, both tilt and non-tilt versions) used in Philips Allura and Azurion medical imaging systems. The affected tables are identified by system codes 722078, 722223, and 722233.
A total of 324 units have been distributed in the United States and 1,390 units internationally across multiple countries worldwide.
During manual repositioning of the patient tabletop, a finger can become trapped between the longitudinal guiding rails and the tabletop, potentially resulting in finger injury to operators and service personnel.
The recalled product
- Product
- Azurion 7 M12 System Code: (1) 722078 (2) 722223 (3) 722233
- Manufacturer
- PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
- Hazard
- finger-entrapment
- pinch-injury
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 (3)
- UDI: (1) 722078 00884838085251(21)
- (2) 722223 00884838099241(21)
- (3) 722233 00884838116764(21)
Distribution
Distributed nationwide across the United States.
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