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.
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.
Particulate found on the Curlin spike.
UDI 38148440000587, Lot/serial numbers: CF1517404, CF1519506, CF1521211, CF1519506, CF1522501, CF1526503, CF1530704, CF1530704, CF1530704, CF1611001, and CF1618152.
Distribution was nationwide. There was government and military distribution. Foreign distribution was made to Canada, Saudi Arabia, Turkey, Croatia, United Arab Emirates, and Australia.
2,417/20-administration set cases