Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-2595-2014 — 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

U.S. FDA — Device Enforcement · United States · 2014-08-05 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2595-2014
Date of alert: 2014-08-05
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Catheter Connections, Inc.
Product category: device
Product type: Devices

Reported risk: 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.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

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