Philips AD7 and AD7X Patient Table Finger Entrapment Risk
The Philips AD7 and AD7X patient tables pose a finger entrapment risk during manual repositioning. Operators and service personnel could sustain finger injuries from the gap between the longitudinal guiding rails and tabletop.
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: Class II medical device recall with a documented mechanical hazard (finger entrapment) but no reported injuries. Per the severity rubric, this qualifies as High (Score 3) as a risk-of-harm product where injury has not yet been reported.
Plain-English summary
The Philips AD7 and AD7X patient tables (available in both tilt and non-tilt versions) are part of the Philips Allura and Azurion systems and are being recalled due to a potential finger entrapment hazard.
During manual repositioning of the patient tabletop, a finger can become entrapped between the longitudinal guiding rails and the tabletop surface. This poses a risk of finger injury to operators and service personnel.
No injuries have been reported to date. The affected devices include 69 units in the United States and 235 units internationally, distributed worldwide. Users should contact Philips for information about remediation options.
The recalled product
- Product
- AlluraXperFD20/15 System Code: (1) 722058
- Manufacturer
- PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
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: 00884838059115(21)
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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