FDA Enforcement Class II Terminated

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, 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.

Recall: Z-0701-2018 · Reported March 7, 2018

Enforcement

Recall Number
Z-0701-2018
Event ID
78573
Classification
Class II
Status
Terminated
Product Type
Devices
Firm
Zevex Incorporated (dba Moog Medical Medical Devices Group)
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
March 7, 2018
Initiation Date
November 10, 2017
Classification Date
February 23, 2018
Termination Date
December 12, 2018
Address
4314 S Zevex Park Ln, N/A, Salt Lake City, UT, 84123-7881, United States

Description

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, 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.

Code Info

UDI 38148440000587, Lot/serial numbers: CF1517404, CF1519506, CF1521211, CF1519506, CF1522501, CF1526503, CF1530704, CF1530704, CF1530704, CF1611001, and CF1618152.

Distribution

Distribution was nationwide. There was government and military distribution. Foreign distribution was made to Canada, Saudi Arabia, Turkey, Croatia, United Arab Emirates, and Australia.

Quantity

2,417/20-administration set cases