Device recall
Z-2319-2026: Mahurkar Elite PASS Trays; Description (Product Number/CFN): 12 FR x 13cm Acute…
FDA device recall · Class II · Mozarc Medical US LLC
Key facts
| Recall number (Z-number) | Z-2319-2026 |
|---|---|
| Recall event | 98891 |
| Product | Mahurkar Elite PASS Trays; Description (Product Number/CFN): 12 FR x 13cm Acute Dual Lumen Catheter with Straight Extensions, PASS Tray (8888221413), 12 FR x 16cm Acute Dual Lumen Catheter with Curved Extensions, PASS Tray (8888222416), 12 FR x 16cm Acute Dual Lumen Catheter with Straight… |
| Product code | MPB |
| Recalling firm | Mozarc Medical US LLC |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K120674 |
| FEI number | 3030574705 |
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