Device recall
Z-0234-04: Mahurkar QPlus Dual Lumen Catheter Insertion Tray with Curved Extension, 13.5…
FDA device recall · Class III · Kendall Healthcare Products Co
Key facts
| Recall number (Z-number) | Z-0234-04 |
|---|---|
| Recall event | 27842 |
| Product | Mahurkar QPlus Dual Lumen Catheter Insertion Tray with Curved Extension, 13.5 Fr/Ch x 19.5cm For hemodialysis, apheresis, and infusion Reference: 8888-135195 |
| Product code | MPB |
| Recalling firm | Kendall Healthcare Products Co |
| Recall class | Class III |
| Status | Terminated |
| Termination date | May 15, 2012 |
| 510(k) numbers | K030209 |
| 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