Device recall
Z-2377-2026: Description/REF: ARTERIAL LINE KIT: SL 20 GA X 5 IN/ASK-04510-MM6 RA CATH KIT…
FDA device recall · Class I · ARROW INTERNATIONAL, LLC
Key facts
| Recall number (Z-number) | Z-2377-2026 |
|---|---|
| Recall event | 98793 |
| Product | Description/REF: ARTERIAL LINE KIT: SL 20 GA X 5 IN/ASK-04510-MM6 RA CATH KIT: 20 GA X 1-3/4IN/NA-04020-X1ASP ACCESS TRAY/ASK-04001-MS RA CATH KIT: 20 GA X 8 CM/ASK-00820-UM1 VESSEL CATH KIT: 20GA X 5IN/AK-04550-S CVC KIT: 1-LUMEN 5 FR X 20 CM/AK-04301-SP CVC KIT: 16 GA X 6IN (16 CM)/AK-04306-SP CVC… |
| Product code | DQY |
| Recalling firm | ARROW INTERNATIONAL, LLC |
| Recall class | Class I |
| Status | Open, Classified |
| 510(k) numbers | K021120, K171146, K810962, K820009, K862056 |
| FEI number | 3013162291 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 Products in the same recall event
- 100–999 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