[Recalled] ImplantDirect, Dental implants intended for use in partially and fully edentulous upper and lower jaws in support of single or multiple-unit restorations and terminal or intermediate abutment support for fixed bridgework. — The m
The product on this page is subject to an official recall. We summarise the regulator's findings and the recommended action.
Recall details
| Product | ImplantDirect, Dental implants intended for use in partially and fully edentulous upper and lower jaws in support of single or multiple-unit restorations and terminal or intermediate abutment support for fixed bridgework. |
|---|---|
| Brand / manufacturer | Implant Direct Sybron Manufacturing, LLC |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-2551-2018 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 03 March 2017 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: The main vial label lists the incorrect part number, but the cap label is correct.
This Class II recall concerns device products distributed in United States 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 Implant Direct Sybron Manufacturing, LLC
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.