Philips Allura patient tables recall due to finger entrapment risk
Philips recalls AD7 and AD7X patient tables in Allura and Azurion systems due to finger entrapment risk during manual repositioning. Operators and service personnel could suffer finger injuries.
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 medical device with an identified risk-of-harm (finger entrapment) during operation, but no reported illnesses or injuries. Meets criteria for High severity: risk-of-harm product where injury has not yet been reported.
Plain-English summary
Philips Medical Systems is recalling the AD7 and AD7X patient tables (both tilt and non-tilt versions) that are part of Philips Allura and Azurion imaging systems. These devices have been distributed worldwide, including throughout the United States and numerous other countries.
During manual repositioning of the patient tabletop, a finger can become trapped between the longitudinal guiding rails and the tabletop. This may result in finger injuries to operators and service personnel who perform equipment repositioning.
The recalled product
- Product
- Allura Xper FD10C System Code: (1) 722001
- Manufacturer
- PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
- Category
- Medical Device — Patient Table
- Affected units
- 1
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)
- UDI: N/A
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 19 recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. 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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