Device recall
Z-0744-03: Tandem-Cath Hemodialysis Cuffed Catheter with side holes 10 Fr 28 cm Arterial…
FDA device recall · Class II · Tyco Healthcare/Kendall
Key facts
| Recall number (Z-number) | Z-0744-03 |
|---|---|
| Recall event | 25817 |
| Product | Tandem-Cath Hemodialysis Cuffed Catheter with side holes 10 Fr 28 cm Arterial Cuff/31 cm Venous Cuff Code #: 8888-228316 |
| Recalling firm | Tyco Healthcare/Kendall |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 12, 2021 |
| 510(k) numbers | K002902 |
At a glance
- 1–9 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