Drug recall
Lubricated Intubating Stylet 6FR that is inserted into an endotracheal tube to facilitate intubation. This…
FDA recall event 70185 · Class II · Cardinal Health
Key facts
| Event ID | 70185 |
|---|---|
| Recall numbers | Z-1054-2015 |
| Recalling firm | Cardinal Health |
| Product type | Devices |
| Products | Lubricated Intubating Stylet 6FR that is inserted into an endotracheal tube to facilitate intubation. This product is used in surgical or medical emergency facilities. Primarily used on infants and… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | A small piece of the stylet sheath has the potential to shear off upon removal of the stylet from the tracheal tube. |
| Initiation date | Dec 23, 2014 |
| Report date | Feb 11, 2015 |
| Termination date | Aug 1, 2016 |
| City | Waukegan |
| State | IL |
| Country | United States |
| FEI number | 3001236905 |
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: