Is PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalled?

Yes — a recall has been published. Reason: Potential Loss of imaging functionality, loss of motorized movement, or loss of data due to unauthorized Hard Disk Drives.

TemporalFDAEn curso

Puede causar daños que por lo general son pasajeros.

Philips Allura, Cardio Vascular-Allura Centron. Model Number: 722400. Interventional Fluoroscopic X-Ray System.

La agencia publicó este retiro solo en inglés. El nombre del producto y los códigos del paquete se muestran tal como los escribió la agencia, para que coincidan exactamente con su paquete.

Revise el dispositivo o su empaque

Model Number: 722400. 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Motivo: Potential Loss of imaging functionality, loss of motorized movement, or loss of data due to unauthorized Hard Disk Drives.La agencia escribió este motivo solo en inglés.La agencia escribió este motivo solo en inglés.
Distribuido: US Nationwide distribution.
Empresa: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Anunciado: 12 de agosto de 2026Esta es la fecha en que se anunció el retiro. La empresa pudo haberlo iniciado semanas antes.
El retiro comenzó: 17 de junio de 2026

Fuente: registro Z-2893-2026 de FDA · consultado el 5 de agosto de 2026

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Cada retiro — de alimentos, medicamentos o dispositivos médicos — se muestra palabra por palabra del aviso oficial de la FDA o del USDA, con un enlace directo. Aquí nada se resume, se reescribe ni se rellena. Este sitio no está afiliado a ninguna agencia del gobierno.