Drug recall
Legacy Full Contour Laboratory Abutment: 3.5mmD Platform/5.5mmD
FDA recall event 77171 · Class II · Implant Direct Sybron Manufacturing, LLC
Key facts
| Event ID | 77171 |
|---|---|
| Recall numbers | Z-2125-2017 |
| Recalling firm | Implant Direct Sybron Manufacturing, LLC |
| Product type | Devices |
| Products | Legacy Full Contour Laboratory Abutment: 3.5mmD Platform/5.5mmD |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Implant Direct Sybron Manufacturing is recalling the Legacy Full-Contour Abutment 3.5mmD Assembly because it may be out of Implant Direct specification. |
| Initiation date | May 2, 2017 |
| Report date | May 31, 2017 |
| Termination date | Jan 8, 2018 |
| City | Westlake Village |
| State | CA |
| Country | United States |
| FEI number | 3001617766 |
At a glance
- 1–9 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: