Drug recall
InterFuse Tail Traction Tool, Part Number 9116. The InterFuse Tail Traction Tool is an optional Class I…
FDA recall event 76275 · Class II · Vertebral Technologies, Inc.
Key facts
| Event ID | 76275 |
|---|---|
| Recall numbers | Z-1151-2017 |
| Recalling firm | Vertebral Technologies, Inc. |
| Product type | Devices |
| Products | InterFuse Tail Traction Tool, Part Number 9116. The InterFuse Tail Traction Tool is an optional Class I non-sterile reusable instrument that can be used to assist with module locking of the InterFuse… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Fit issues have been identified with the Tail Traction Tool (PN 9116) when used with the Interfuse T tailed implant. The InterFuse T Tail may not fit into the Thru Hole in the instrument. |
| Initiation date | Jan 13, 2017 |
| Report date | Feb 15, 2017 |
| Termination date | Oct 5, 2017 |
| City | Minneapolis |
| State | MN |
| Country | United States |
| FEI number | 3007617183 |
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: