Device recall
Z-1917-2026: Arrowg+ard Blue MAC" Two-Lumen Central Venous Access Kit for use with 7.5 - 8…
FDA device recall · Class II · ARROW INTERNATIONAL, LLC
Key facts
| Recall number (Z-number) | Z-1917-2026 |
|---|---|
| Recall event | 98618 |
| Product | Arrowg+ard Blue MAC" Two-Lumen Central Venous Access Kit for use with 7.5 - 8 Fr. Catheters REF ASK-21142-DMC UDI code: (01)10801902218930(17)270630(11)251211(10)33F25M0671 The MAC Multi-Lumen Central Venous Access Device with Arrowg+ard Blue technology permits short-term (<30 days) venous access… |
| Product code | OFC |
| Recalling firm | ARROW INTERNATIONAL, LLC |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3013162291 |
At a glance
- None 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