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

Recall Z-2614-2018 — Lopez Valve¿, Sterile The blood tubing accessory with CLAVE Connector is a single use, sterile, non-pyrogenic device intended for use as an adjunct to blood tubing sets or venipuncture devices for needle-free withdrawal of blood.

U.S. FDA — Device Enforcement · United States · 2017-07-31 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2614-2018
Date of alert
2017-07-31
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
ICU Medical, Inc.
Product category
device
Product type
Devices
Reported risk: Some devices were labeled as Does not contain DEHP even though the product may contain small amounts of DEHP.
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.

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