FDA Device recall Z-0697-2018

MOOG Curlin Infusion Administration Set, Ref 340-4114, Non-DEHP Microbore Tubing with Non-Vented Bag Spike, packaged 20/box, for use with t…

FDA Device
Class II
terminated
Published 2018-03-07

On 2018-03-07 the FDA classified a Class II recall of MOOG Curlin Infusion Administration Set, Ref 340-4114, Non-DEHP Microbore Tubing with Non-Vented Bag Spike, packaged 20/box, for use with t… by Zevex Dba Moog Medical Medical Devices Group, citing particulate found on the Curlin spike.

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-0697-2018
Classification	Class II
Status	terminated
Initiated	2017-11-10
Published	2018-03-07
Last updated	2026-09-13 11:54 UTC
Company	Zevex Dba Moog Medical Medical Devices Group
Distribution	US

Product

MOOG Curlin Infusion Administration Set, Ref 340-4114, Non-DEHP Microbore Tubing with Non-Vented Bag Spike, packaged 20/box, for use with the MOOG Curlin Ambulatory Volumetric Infusion Pump, RX, 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.

Reason

Particulate found on the Curlin spike.

Identifiers

code_info	UDI 38148440000396, Lot/serial numbers: CF1514703, CF1514702, CF1514702, CF1514701, CF1514702, CF1517405, CF1517406, CF… UDI 38148440000396, Lot/serial numbers: CF1514703, CF1514702, CF1514702, CF1514701, CF1514702, CF1517405, CF1517406, CF1518301, CF1518302, CF1518303, CF1518301, CF1521101, CF1521103, CF1521102, CF1521701, CF1522306, CF1522308, CF1522307, CF1523312, CF1524407, CF1524407, CF1525101, CF1524407, CF1525103, CF1525102, CF1526505, CF1526506, CF1527307, CF1527306, CF1528011, CF1528607, CF1528606, CF1529306, CF1529307, CF1530106, CF1530707, CF1530706, CF1530706, CF1530705, CF1530706, CF1530707, CF1530706, CF1530707, CF1532102, CF1531406, CF1532102, CF1531405, CF1532975, CF1532976, CF1532976, CF1532976, CF1532976, CF1535001, CF1533504, CF1534902, CF1535666, CF1600507, CF1600508, CF1601203, CF1601903, CF1602604, CF1603304, CF1604704, CF1605406, CF1606104, CF1607504, CF1610405, CF1611003, CF1612404, CF1613105, CF1613804, CF1615209, CF1616608, and CF1616608.

code_info

UDI 38148440000396, Lot/serial numbers: CF1514703, CF1514702, CF1514702, CF1514701, CF1514702, CF1517405, CF1517406, CF…

UDI 38148440000396, Lot/serial numbers: CF1514703, CF1514702, CF1514702, CF1514701, CF1514702, CF1517405, CF1517406, CF1518301, CF1518302, CF1518303, CF1518301, CF1521101, CF1521103, CF1521102, CF1521701, CF1522306, CF1522308, CF1522307, CF1523312, CF1524407, CF1524407, CF1525101, CF1524407, CF1525103, CF1525102, CF1526505, CF1526506, CF1527307, CF1527306, CF1528011, CF1528607, CF1528606, CF1529306, CF1529307, CF1530106, CF1530707, CF1530706, CF1530706, CF1530705, CF1530706, CF1530707, CF1530706, CF1530707, CF1532102, CF1531406, CF1532102, CF1531405, CF1532975, CF1532976, CF1532976, CF1532976, CF1532976, CF1535001, CF1533504, CF1534902, CF1535666, CF1600507, CF1600508, CF1601203, CF1601903, CF1602604, CF1603304, CF1604704, CF1605406, CF1606104, CF1607504, CF1610405, CF1611003, CF1612404, CF1613105, CF1613804, CF1615209, CF1616608, and CF1616608.

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0697-2018%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.