Device recall
Z-1955-2019: MAHURKAR and Argyle acute hemodialysis catheters, Material numbers 8813793009…
FDA device recall · Class II · COVIDIEN LLC
Key facts
| Recall number (Z-number) | Z-1955-2019 |
|---|---|
| Recall event | 82802 |
| Product | MAHURKAR and Argyle acute hemodialysis catheters, Material numbers 8813793009 8813793013 8813794005 8813794009 8813816005 8813816009 8813817005 8813817009 8815668007 8815668011 8815668021 8815668027 8817142005 8817143005 8817145005 8817146001 8817146007 8817149007 8817232018 8817232019 8817277007… |
| Product code | NIE |
| Recalling firm | COVIDIEN LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 9, 2024 |
| 510(k) numbers | K020089, K030209, K102605 |
| FEI number | 1282497 |
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