DualCap IV Pole Strips Disinfectant Caps for Luer Access Valves — Class II medical device recall Z-2595-2014
Terminated recall by Catheter Connections, Inc., reported 2014-09-17, distributed in CT, GA, MD, PA. Catheter Connections is recalling DualCap IV Pole Strips disinfectant caps for luer access valves due to poten
| Recall number | Z-2595-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Catheter Connections, Inc., Salt Lake City, UT, United States |
| Recall initiated | 2014-08-05 |
| Classified | 2014-09-05 |
| Reported by FDA | 2014-09-17 |
| Terminated | 2014-10-08 |
| Distributed | CT, GA, MD, PA |
| Quantity | 24,910 units |
| Reason classes | sterility, packaging |
| Lot numbers | 1406509 |
| Model numbers | 500-LB |
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 for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2595-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.