Safety
Recalls & safety notices
Official recall records linked to the implant systems in our database, with the affected product and the reason in plain words.
Please read before drawing conclusions: a recall usually affects one product reference or batch, often for a labeling or packaging issue. It does not mean the whole brand is unsafe. Recall counts can't be used to rank brands.
| System | Recall number | Product | Reason | Root cause (FDA) | Initiated | Status |
|---|---|---|---|---|---|---|
| NobelActive | Z-2207-2020 | NobelActive Internal NP 3.5x15mm, REF 34128 | Top label could state 11.5 mm length for an implant that is actually 15 mm long. | Labeling mix-ups | 19 Jul 2019 | Terminated |
Searches performed
| System | Query | Date | Results |
|---|---|---|---|
| Straumann BLX | product_description:BLX | 27 Sept 2026 | 0 |
| NobelActive | product_description:NobelActive | 27 Sept 2026 | 1 |
| Osstem TSIII | product_description:TSIII | 27 Sept 2026 | 0 |
| MegaGen AnyRidge | product_description:AnyRidge | 27 Sept 2026 | 0 |
Source: FDA device recall database via openFDA. EU field safety notices (EUDAMED / national agencies) will be added. We don't turn MAUDE adverse-event reports into brand comparisons: they are unverified, incomplete and can't show how often problems happen.