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[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

recall fda device united-states

The product on this page is subject to an official recall. We summarise the regulator's findings and the recommended action.

Recall details

ProductImplantDirect, 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 / manufacturerImplant Direct Sybron Manufacturing, LLC
Categorydevice
Issuing authorityFDA_DEVICE
ReferenceZ-2551-2018
Country of noticeUnited States
Risk levelClass II
Hazard typerecall
Notice date03 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.

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