Drug recall
Medtronic Navigated Cannulated Taps Individual cannulated taps are packaged in a clear plastic tube with…
FDA recall event 71342 · Class II · Medtronic Navigation, Inc.
Key facts
| Event ID | 71342 |
|---|---|
| Recall numbers | Z-1847-2015 |
| Recalling firm | Medtronic Navigation, Inc. |
| Product type | Devices |
| Products | Medtronic Navigated Cannulated Taps Individual cannulated taps are packaged in a clear plastic tube with protective plastic end caps. Kit/sets contain various devices including the taps. The kit/set… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Medtronic Navigation is initiating a field correction due to the potential for injury which could occur as a result of cleaning the Medtronic Navigated Cannulated Taps. |
| Initiation date | May 26, 2015 |
| Report date | Jul 8, 2015 |
| Termination date | Oct 23, 2015 |
| City | Louisville |
| State | CO |
| Country | United States |
| FEI number | 1000517638 |
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: