Device recall
Z-2527-2015: Mahurkar Acute Dual Lumen Catheter Tray, High Flow Pre-Curved with IC* Safety…
FDA device recall · Class II · Covidien LLC
Key facts
| Recall number (Z-number) | Z-2527-2015 |
|---|---|
| Recall event | 71893 |
| Product | Mahurkar Acute Dual Lumen Catheter Tray, High Flow Pre-Curved with IC* Safety Components, 13.5 FR x 13.5 cm Item Code: 8888135139 Product Usage: Sterile Delivery are indicated for use in flushing compatible intravenous administration sets and indwelling intravascular access devices. |
| Product code | NGT |
| Recalling firm | Covidien LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 29, 2017 |
| 510(k) numbers | K060339 |
| FEI number | 1219930 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 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