Drug recall
Aesculap Inc.(AIC) Miethke Ventricular Catheter with Deflector/Miethke Shunt System The Miethke Shunt System…
FDA recall event 68091 · Class II · Aesculap, Inc.
Key facts
| Event ID | 68091 |
|---|---|
| Recall numbers | Z-1676-2014 |
| Recalling firm | Aesculap, Inc. |
| Product type | Devices |
| Products | Aesculap Inc.(AIC) Miethke Ventricular Catheter with Deflector/Miethke Shunt System The Miethke Shunt System is intended to shut cerebrospinal fluid from the lateral ventricles of the brain into the… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | AIC (USA) received information regarding 3 complaints in which the deflector did not move freely on the ventricular catheter. |
| Initiation date | Apr 21, 2014 |
| Report date | Jun 11, 2014 |
| Termination date | Oct 20, 2014 |
| City | Center Valley |
| State | PA |
| Country | United States |
| FEI number | 2916714 |
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: