FDANovember 10, 2017device

MOOG Curlin Infusion Administration Set, Ref 340-4168, Non-DEHP Microbore Tubing with Non-Vented Bag Spike and distal Female Luer Y-Site with Check Valve, Anti-Siphon Valve included for Free Flow Protection, packaged 20/box, for use with the Moog Curlin Ambulatory Volumetric Infusion Pump, RX, St...

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Particulate found on the Curlin spike.

What to do

FDA enforcement status: Terminated

Brands named

zevex incorporated dba moog medical medical devices groupzevexzevex incorporated

UPCs

38148440000587

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

Own something like this?

AllClear screens your whole list against every CPSC, FDA, USDA and NHTSA recall — and tells you the day a new one names something you own.

Start free — 200 items, no card →