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

Recall Z-0698-2018 — MOOG Curlin Infusion Administration Set, Ref 340-4133, Non-DEHP Microbore Tubing with Non-Vented Bag Spike and Needleless Injection Port (Positive Pressure), packaged 20/box, for use with the Moog Curlin Ambulatory Volumetric Infusion Pump, RX, Sterile. Product Usage: Administration set to be u

U.S. FDA — Device Enforcement · United States · 2017-11-10 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-0698-2018
Date of alert: 2017-11-10
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Zevex Incorporated (dba Moog Medical Medical Devices Group)
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 38148440000488

Reported risk: Particulate found on the Curlin spike.

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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