Drug recall
3.0/4.0 Cannulated Drill Bit; a component of the Tiger Cannulated Screw System The Tiger Cannulated Screw…
FDA recall event 71812 · Class II · Trilliant Surgical Ltd.
Key facts
| Event ID | 71812 |
|---|---|
| Recall numbers | Z-2452-2015 |
| Recalling firm | Trilliant Surgical Ltd. |
| Product type | Devices |
| Products | 3.0/4.0 Cannulated Drill Bit; a component of the Tiger Cannulated Screw System The Tiger Cannulated Screw Fixation System implants are intended for fixation of fractures, non-unions, arthrodesis and… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | The cannulation of the 3.0/4.0 Cannulated Drill Bit inner diamter is too small to allow for the guide wire to pass completely through. |
| Initiation date | Jul 20, 2015 |
| Report date | Sep 2, 2015 |
| Termination date | Jan 26, 2017 |
| City | Houston |
| State | TX |
| Country | United States |
| FEI number | 3007420745 |
At a glance
- 1–9 Products in this recall
- 1–9 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: