Drug recall
Salto Talaris Tibial Guide, Part # MJU333,Tray/Kit Code YKAL11, Non sterile. Orthopedic Manual Surgical…
FDA recall event 71913 · Class II · Tornier, Inc
Key facts
| Event ID | 71913 |
|---|---|
| Recall numbers | Z-2465-2015 |
| Recalling firm | Tornier, Inc |
| Product type | Devices |
| Products | Salto Talaris Tibial Guide, Part # MJU333 ,Tray/Kit Code YKAL11, Non sterile. Orthopedic Manual Surgical Instrument |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Tornier has initiated a voluntary recall for the Salto Talaris Tibial Guide (part number MJU333) due to a complaint that occurred during physician training, that the guide cannot be assembled to the… |
| Initiation date | Aug 6, 2015 |
| Report date | Sep 2, 2015 |
| Termination date | Apr 8, 2016 |
| City | Bloomington |
| State | MN |
| Country | United States |
| FEI number | 3000718467 |
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: