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.
Class I - DangerousWhat Should You Do?
- Check if you have this product: 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.
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- Report problems: Report any issues to the FDA's Safety Reporting Portal.
⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.
Recall Details
- Company:
- Zevex Incorporated (dba Moog Medical Medical Devices Group)
- Reason for Recall:
- Particulate found on the Curlin spike.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
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.
Product Codes/Lot Numbers:
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.
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-0697-2018
Related Recalls
MOOG Curlin Infusion Administration Set, Ref 340-4133, Non-DEHP Microbore Tubing with Non-Vented Bag Spike and Needleless Injection Port (Positive Pressure), 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.
Zevex Incorporated (dba Moog Medical Medical Devices Group)
Particulate found on the Curlin spike.
MOOG Curlin Infusion Administration Set, Ref 340-4134, Non-DEHP Microbore Tubing with Non-Vented Bag Spike and Y-Site with Check Valve, 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.
Zevex Incorporated (dba Moog Medical Medical Devices Group)
Particulate found on the Curlin spike.
MOOG Curlin Infusion Administration Set, Ref 340-4169, Non-DEHP Microbore Tubing with Non-Vented Bag Spike and distal Ultrasite Needleless Injection Port (Positive Pressure), 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.
Zevex Incorporated (dba Moog Medical Medical Devices Group)
Particulate found on the Curlin spike.