Zevex Incorporated (dba MOOG Medical Devices Group) recalls MOOG Curlin Infusion Administration Set, REF 340-4130, Non-DEHP Tubing with Non-Vented Bag Spike and Vented 0.2 Micron…

Recall date

February 27, 2019

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-2053-2019

FDA classification

Class II

Brand / firm

Zevex Incorporated (dba MOOG Medical Devices Group)

Sold / distributed

Distribution was made to GA, IL, KS, MA, MI, and OH. There was no foreign/military/government distribution.

Why it was recalled

Administration sets leaked at the filter.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

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, epidural, subcutaneous, or enteral infusions.