Device recall
Z-0715-2013: Medisystems 17 Gauge x 1" inch AV Fistula Needle Product Code: D9-2007MGLB…
FDA device recall · Class II · Medisystems a NX Stage Company
Key facts
| Recall number (Z-number) | Z-0715-2013 |
|---|---|
| Recall event | 63959 |
| Product | Medisystems 17 Gauge x 1" inch AV Fistula Needle Product Code: D9-2007MGLB Product Usage: Medisystems AVF with MasterGuard anti-stick needle protector is indicated for use as a vascular access device in hemodialysis or other extracorporeal procedures. It is intended for use in conjunction with a… |
| Product code | FIE |
| Recalling firm | Medisystems a NX Stage Company |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 10, 2013 |
| 510(k) numbers | K910734 |
| FEI number | 3003464075 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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