Drug recall
CareFusion Vital Signs LightWand Stylet. A device inserted into an endotracheal tube to aid in the intubation…
FDA recall event 70753 · Class II · Vital Signs Colorado Inc.
Key facts
| Event ID | 70753 |
|---|---|
| Recall numbers | Z-1556-2015, Z-1557-2015 |
| Recalling firm | Vital Signs Colorado Inc. |
| Product type | Devices |
| Products | CareFusion Vital Signs LightWand Stylet. A device inserted into an endotracheal tube to aid in the intubation procedure., Introduction Pack. A device inserted into an endotracheal tube to aid in the intubation procedure. |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Vital Signs Colorado (dba CareFusion) is recalling Vital Signs LightWand Stylet catalog numbers 3910 and 3960 due to a potential patient safety risk involving a breach in the sterile packaging that… |
| Initiation date | Mar 13, 2015 |
| Report date | May 6, 2015 |
| Termination date | Oct 7, 2015 |
| City | Englewood |
| State | CO |
| Country | United States |
| FEI number | 1718887 |
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: