Drug recall
Low Profile Abutment, Non-Hexed Castable Cylinder Model LPCCC1. Product is labeled in part: "***REF…
FDA recall event 62578 · Class II · Biomet 3i, LLC
Key facts
| Event ID | 62578 |
|---|---|
| Recall numbers | Z-2271-2012 |
| Recalling firm | Biomet 3i, LLC |
| Product type | Devices |
| Products | Low Profile Abutment, Non-Hexed Castable Cylinder Model LPCCC1. Product is labeled in part: "***REF LPCCC1***Low profile Abutment Hexed Castable Cylinder***Cylinder; Cylindre; Zylinder; Cilindro… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Biomet 3i conducted a recall on the device Low Profile Abutment, Non-Hexed Castable Cylinder due to some packages labeled LPCCC1, Hexed Castable Cylinder possibly containing LPCCC2, Non-Hexed Castable… |
| Initiation date | May 31, 2012 |
| Report date | Sep 5, 2012 |
| Termination date | Nov 21, 2013 |
| City | Palm Beach Gardens |
| State | FL |
| Country | United States |
| FEI number | 1038806 |
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: