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FDA (Device enforcement)Recalled 2025-01-13class ii

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.: AlluraXper FD20 System Code: (1) 722006 (2) 722012 (3) 722028

Hazard

Potential safety issue with the AD7 and AD7X patient tables (both tilt and non-tilt versions) part of the Philips Allura and Azurion systems. During manual repositioning of the patient tabletop, a finger can get entrapped between the longitudinal guiding rails and the tabletop. This may result in an injury of the finger, applicable for operators and service personnel

Details from the source

Reason for recall: Potential safety issue with the AD7 and AD7X patient tables (both tilt and non-tilt versions) part of the Philips Allura and Azurion systems. During manual repositioning of the patient tabletop, a finger can get entrapped between the longitudinal guiding rails and the tabletop. This may result in an injury of the finger, applicable for operators and service personnel Distribution: Worldwide distribution - US Nationwide and the countries of Canada, Afghanistan, Albania, Algeria, Argentina, Armenia, Australia, Austria, Azerbaijan, Bahrain, Bangladesh, Belarus, Belgium, Bolivia, Bosnia and Herzegovina, Brazil, Brunei Darussalam, Bulgaria, Cambodia, Cayman Islands, Chile, China, Colombia, Costa Rica, C¿te D'Ivoire, Croatia, Cuba, Cyprus, Czech Republic, Denmark, Dominican Repub Quantity: 1528 units US; 3482 units OUS Lot/code info: UDI: (1) 722006 00884838055513(21) 00884838059115(21) 00884838059191(10) (2) 722012 00884838059054(21) (3) 722028 00884838054202(21)

UPC codes

00884838055513, 00884838059115, 00884838059191, 00884838059054, 00884838054202

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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