Device recall
Z-1007-2018: MAHURKAR"* Elite 12 FR x 16cm Acute Dual Lumen Dialysis Catheter with Curved…
FDA device recall · Class II · Medtronic Minimally Invasive Therapies Group
Key facts
| Recall number (Z-number) | Z-1007-2018 |
|---|---|
| Recall event | 79319 |
| Product | MAHURKAR"* Elite 12 FR x 16cm Acute Dual Lumen Dialysis Catheter with Curved Extensions, IC Trays. Product Number: 8888222316. |
| Product code | MPB |
| Recalling firm | Medtronic Minimally Invasive Therapies Group |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 15, 2018 |
| 510(k) numbers | K120674 |
| FEI number | 1282497 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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