Official recall record

Philips Azurion 7 M20. Model Numbers: 722079, 722224, 722282.

US FDA — Medical Devices · 2026-10-06 · NetherlandsClass II

Issuing authority: US FDA — Medical Devices
Recall initiated by firm: 2026-10-06
Country of alert: Netherlands
Alert level: Class II
Alert type: recall
Barcode (EAN/GTIN): 00884838085268
Brand on record: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

What the authority reported

Solid-State Drives (SSDs) that are not specified in the Medical Device File may have been installed in various PCs. These SSDs may have different performance characteristics, which may include reduced reliability over time such as loss of imaging functionality or motorized movement, a blank or black display, and/or the inability to store newly acquired images or access previously acquired images.

What to do

Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.

Verify at the source: US FDA — Medical Devices — official record →
Record last checked against the registry on 2026-11-13.

More recalls: US FDA — Medical Devices · Netherlands · all filters

Same barcode in other registries

The same EAN appears in 5 other official recall record(s) — a cross-border signal worth checking if you bought this product abroad.

2023-06-12 · US FDA — Medical Devices
Azurion 7 M20. X-ray Image guided Therapy System.
2023-12-08 · US FDA — Medical Devices
Azurion 7 M20 FlexArm system (Software version R2.x) with Maquet Magnus Table (Software version 05.02.12)
2025-01-13 · US FDA — Medical Devices
Azurion 7 M20; Catalog numbers: (1) 722079, (2) 722224, (3) 722234, (4) 722282 (OUS ONLY);
2025-06-04 · US FDA — Medical Devices
Azurion 7 M20. Fluoroscopic X-Ray System.
2024-08-06 · US FDA — Medical Devices
Philips Azurion 7M20 systems with FlexArm ceiling-mounted system, Interventional Fluoroscopic X-Ray System, Model Number

Other recalls from this brand

2026-10-06 · US FDA — Medical Devices
Philips Azurion 5 M20. Model Numbers: 722228, 722281.
2026-10-06 · US FDA — Medical Devices
Philips Azurion S. Model Number: 722285.
2026-10-06 · US FDA — Medical Devices
Philips Azurion 3 M12. Model Numbers: 722063, 722221.

All 90 official recall notices naming PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. on this site →

ProductGuru Recalls republishes official safety information with attribution. We are not the issuing authority and this page is not advice. If this product is a medical device or medication, speak to a doctor or pharmacist. Found an error? Report it — corrections are published.