[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
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
| Product | Azurion 7 B12 System Model Numbers:(1) 722067, (2) 722225, (3) 722235; Software Version Number - All versions: R1.X, R2.X, R3.X |
|---|---|
| Brand / manufacturer | PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-1346-2026 |
| Country of notice | Netherlands |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 26 January 2026 |
| EAN / barcode | 884838085350 |
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 →
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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.