Device recall
Z-0745-03: Tandem-Cath Hemodialysis Cuffed Catheter with no side holes 10 Fr 19 cm Arterial…
FDA device recall · Class II · Tyco Healthcare/Kendall
Key facts
| Recall number (Z-number) | Z-0745-03 |
|---|---|
| Recall event | 25817 |
| Product | Tandem-Cath Hemodialysis Cuffed Catheter with no side holes 10 Fr 19 cm Arterial Cuff/22cm Venous Cuff Code #: 8888-219220 |
| Recalling firm | Tyco Healthcare/Kendall |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 12, 2021 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
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