Drug recall
Thin-Flex Venous Cannula, Model Number:TF292902A
FDA recall event 72667 · Class II · Edwards Lifesciences, LLC
Key facts
| Event ID | 72667 |
|---|---|
| Recall numbers | Z-0398-2016 |
| Recalling firm | Edwards Lifesciences, LLC |
| Product type | Devices |
| Products | Thin-Flex Venous Cannula, Model Number:TF292902A |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Edwards Lifesciences initiated a field action for the Thin-Flex Venous Cannula (Model TF292902A) because the connector size is incorrectly described in the Edwards product guide as 3/8 inch. The… |
| Initiation date | Nov 4, 2015 |
| Report date | Dec 16, 2015 |
| Termination date | Feb 10, 2017 |
| City | Draper |
| State | UT |
| Country | United States |
| FEI number | 1713910 |
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: