FDA Device recall Z-2893-2026

Philips Allura, Cardio Vascular-Allura Centron

• FDA Device
• Class II
• ongoing
• Published 2026-08-12

On 2026-08-12 the FDA classified a Class II recall of Philips Allura, Cardio Vascular-Allura Centron by Philips Medical Systems Nederland B V, citing potential Loss of imaging functionality, loss of motorized movement, or loss of data due to unauthorized Hard Disk Drives.

Read the official FDA Device notice

Product

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

Reason

Potential Loss of imaging functionality, loss of motorized movement, or loss of data due to unauthorized Hard Disk Drives.

Identifiers

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:58 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2893-2026%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.