Drug recall
Telluride Percutaneous Rod Inserter Long, Model #7706-1904. The Inserter is a reusable device provided within…
FDA recall event 70376 · Class II · Biomet Spine, LLC
Key facts
| Event ID | 70376 |
|---|---|
| Recall numbers | Z-1089-2015 |
| Recalling firm | Biomet Spine, LLC |
| Product type | Devices |
| Products | Telluride Percutaneous Rod Inserter Long, Model #7706-1904. The Inserter is a reusable device provided within an aluminum sterilization case along with other orthopedic manual surgical instruments… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | The Telluride Percutaneous Rod Inserter Long does not contain a feature that locks the Rod in place during use. There is a potential for the Rod to disengage from the Inserter during insertion, and… |
| Initiation date | Dec 19, 2011 |
| Report date | Feb 18, 2015 |
| Termination date | Mar 23, 2015 |
| City | Broomfield |
| State | CO |
| Country | United States |
| FEI number | 3004485144 |
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: