Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
MOOG Curlin Infusion Administration Set Recalled by Zevex Incorporated (dba Moog Medical Medical Devices Group) Due to Particulate found on the Curlin spike.
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Zevex Incorporated (dba Moog Medical Medical Devices Group) directly.
Affected Products
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.
Quantity: 2,497/20-administration set cases
Why Was This Recalled?
Particulate found on the Curlin spike.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Zevex Incorporated (dba Moog Medical Medical Devices Group)
Zevex Incorporated (dba Moog Medical Medical Devices Group) has 6 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report