Device recall
Z-0630-2018: Central Venous Catheter Set Triple Lumen Polyurethane, Catalog Identifier…
FDA device recall · Class II · Cook Inc.
Key facts
| Recall number (Z-number) | Z-0630-2018 |
|---|---|
| Recall event | 79050 |
| Product | Central Venous Catheter Set Triple Lumen Polyurethane, Catalog Identifier: C-UTLM-501J Product Usage: The central venous catheter is designed for treatment of critically ill patients and is suggested for: 1. Continuous or intermittent drug infusions; 2. Central venous blood pressure monitoring… |
| Product code | FOZ |
| Recalling firm | Cook Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 8, 2019 |
| 510(k) numbers | K173416 |
| FEI number | 1820334 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 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