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[Recalled] Azurion 7 B12 System Model Numbers:(1) 722067, (2) 722225, (3) 722235; Software Version Number - All versions: R1.X, R2.X, R3.X — Under certain conditions, the table may move unexpectedly when the Reset Geomet… | FDA 2026-01-26

recall fda device netherlands

A safety authority has issued a recall or warning for this item. The confirmed facts from the source notice are laid out below.

Recall details

ProductAzurion 7 B12 System Model Numbers:(1) 722067, (2) 722225, (3) 722235; Software Version Number - All versions: R1.X, R2.X, R3.X
Brand / manufacturerPHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Categorydevice
Issuing authorityFDA_DEVICE
ReferenceZ-1346-2026
Country of noticeNetherlands
Risk levelClass II
Hazard typerecall
Notice date26 January 2026
EAN / barcode884838085350

Why it was recalled

According to the FDA_DEVICE notice, the identified hazard is: Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active.

This Class II recall concerns device products distributed in Netherlands and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.

What to do if you own this product

Check whether your unit is affected and follow the authority's guidance before further use.

Read the full official notice →

Related recalls from PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.

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