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

Recall Z-2053-2019 — MOOG Curlin Infusion Administration Set, REF 340-4130, Non-DEHP Tubing with Non-Vented Bag Spike and Vented 0.2 Micron Filter, packaged 20 sets/carton, sterile. Product Usage: Administration set to be used with the Moog Curlin Infusion Pump. The pump can be used for intravenous, intra-arterial,

U.S. FDA — Device Enforcement · United States · 2019-02-27 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2053-2019
Date of alert: 2019-02-27
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Zevex Incorporated (dba MOOG Medical Devices Group)
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 38148440000464

Reported risk: Administration sets leaked at the filter.

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

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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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