Drug recall
RePlant¿ Angled Abutment Part Number 6050-52-60
FDA recall event 74624 · Class II · Implant Direct Sybron Manufacturing, LLC
Key facts
| Event ID | 74624 |
|---|---|
| Recall numbers | Z-2320-2016 |
| Recalling firm | Implant Direct Sybron Manufacturing, LLC |
| Product type | Devices |
| Products | RePlant¿ Angled Abutment Part Number 6050-52-60 |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Issue with design specification; oversized condition. |
| Initiation date | Jul 5, 2016 |
| Report date | Aug 10, 2016 |
| Termination date | Feb 16, 2017 |
| 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: