Philips Azurion and Allura System Patient Tables: Finger Entrapment Risk
Philips Azurion and Allura system patient tables may trap fingers between the guiding rails and tabletop during manual repositioning, risking finger injury to operators and service personnel.
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: This FDA Class II medical device recall involves a risk-of-harm hazard (finger entrapment) with no reported injuries to date. The source text describes only the potential for finger injury, placing it in the 'risk-of-harm products where injury has not yet been reported' category per the severity rubric.
Plain-English summary
The Azurion 7 B12 system patient tables (AD7 and AD7X models, both tilt and non-tilt versions) from Philips are being recalled due to an entrapment hazard. During manual repositioning of the patient tabletop, fingers can become entrapped between the longitudinal guiding rails and the tabletop, creating a risk of finger injury.
The recall affects 90 units distributed in the United States and 458 units distributed internationally across numerous countries. Operators and service personnel who manually reposition these patient tables are at risk of finger entrapment injury.
The recalled product
- Product
- Azurion 7 B12 System Code: (1) 722067 (2) 722225 (3) 722235
- 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) 722067 00884838085350(21)
- (2) 722225 00884838099265(21)
- (3) 722235 00884838116788(21)
Distribution
Distributed nationwide across the United States.
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