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

Recall Z-2331-2017 — 1) Pressure Injectable ARROW(R) PICC Kit with Chlorag+ard(R) Technology The Pressure Injectable PICC with Chlorag+ard Antimicrobial and Antithrombogenic Technology is indicated for short-term or long-term peripheral access to the central venous system for intravenous therapy, blood sampling, infusi

U.S. FDA — Device Enforcement · United States · 2017-05-09 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2331-2017
Date of alert: 2017-05-09
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Arrow International Inc
Product category: device
Product type: Devices

Reported risk: Arrow International is recalling the affected product because the packaging may not be completely sealed, which may compromise sterility.

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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