Drug recall
Miethke Shunt System accessories Product Usage: - The Miethke Shunt System is intended to shut cerebrospinal…
FDA recall event 70086 · Class II · Aesculap, Inc.
Key facts
| Event ID | 70086 |
|---|---|
| Recall numbers | Z-1012-2015 |
| Recalling firm | Aesculap, Inc. |
| Product type | Devices |
| Products | Miethke Shunt System accessories Product Usage: - The Miethke Shunt System is intended to shut cerebrospinal fluid from the lateral ventricles of the brain into the peritoneum. |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Some Miethke Shunt System accessories may have an incorrect MR safety symbol on the shelf box label. The label should have NO symbol but instead is marked with the MR conditional symbol. The product… |
| Initiation date | Dec 17, 2014 |
| Report date | Feb 4, 2015 |
| Termination date | Dec 13, 2016 |
| 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: