FDA Device recall Z-2595-2014
DualCap IV Pole Strips Disinfectant Caps for Luer Access Valves, REF 500-LB, Sterile
- FDA Device
- Class II
- terminated
- Published 2014-09-17
On 2014-09-17 the FDA classified a Class II recall of DualCap IV Pole Strips Disinfectant Caps for Luer Access Valves, REF 500-LB, Sterile by Catheter Connections, citing catheter Connections is recalling DualCap IV Pole Strips disinfectant caps for luer access valves due to potential improper packaging cap seal which may render the sealed cap non-….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2595-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-08-05 |
| Published | 2014-09-17 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Catheter Connections |
| Distribution | CT, GA, MD, PA |
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 not removed.
Reason
Catheter Connections is recalling DualCap IV Pole Strips disinfectant caps for luer access valves due to potential improper packaging cap seal which may render the sealed cap non-sterile.
Identifiers
| code_info | Lot 1406509 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2595-2014%22
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