Drug recall
TUNNELOC ROUND HEAD INTERFERENCE SCREW 8MMX25MM Biomet Sports Medicine manufactures a variety of internal…
FDA recall event 64004 · Class II · Biomet, Inc.
Key facts
| Event ID | 64004 |
|---|---|
| Recall numbers | Z-0753-2013 |
| Recalling firm | Biomet, Inc. |
| Product type | Devices |
| Products | TUNNELOC ROUND HEAD INTERFERENCE SCREW 8MMX25MM Biomet Sports Medicine manufactures a variety of internal fixation devices intended to aid in arthroscopic and orthopedic reconstructive procedures… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Thru hole at the tip of the screw is undersized. |
| Initiation date | Jan 3, 2013 |
| Report date | Feb 6, 2013 |
| Termination date | Aug 2, 2013 |
| City | Warsaw |
| State | IN |
| Country | United States |
| FEI number | 1825034 |
At a glance
- 1–9 Products in this recall
- None 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: