Device recall
Z-0805-2013: Aesculap(R) - Miethke Shunt System, FT040T - Control Reservoir Set w/Distal…
FDA device recall · Class II · Aesculap, Inc.
Key facts
| Recall number (Z-number) | Z-0805-2013 |
|---|---|
| Recall event | 63244 |
| Product | Aesculap(R) - Miethke Shunt System, FT040T - Control Reservoir Set w/Distal Catheter and FT075P 0 Ventric Cathet, w/Stylet and RT-ANG Guide Central Nervous System Shunt and Components intended to shunt cerebrospinal fluid (CSF) from the lateral ventricles of the brain into the peritoneum. |
| Product code | JXG |
| Recalling firm | Aesculap, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 8, 2014 |
| 510(k) numbers | K0110030 |
| FEI number | 2916714 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database