Device recall
Z-2595-2014: DualCap IV Pole Strips Disinfectant Caps for Luer Access Valves, REF 500-LB…
FDA device recall · Class II · Catheter Connections, Inc.
Key facts
| Recall number (Z-number) | Z-2595-2014 |
|---|---|
| Recall event | 69066 |
| Product | DualCap IV Pole Strips Disinfectant Caps for Luer Access Valves, REF 500-LB, Sterile. When left in place for five (5) minutes DualCap Solo" disinfects needleless luer access valves; thereafter the caps provide a physical barrier to contamination up to ninety-six (96) hours under normal conditions if… |
| Product code | LKB |
| Recalling firm | Catheter Connections, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 8, 2014 |
| 510(k) numbers | K123065 |
| FEI number | 3009141010 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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