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 Devices Group) Due to Administration sets leaked at the filter.
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 Devices Group) directly.
Affected Products
MOOG Curlin Infusion Administration Set, REF 340-4130, Non-DEHP Tubing with Non-Vented Bag Spike and Vented 0.2 Micron Filter, packaged 20 sets/carton, 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: 569/20-set caess
Why Was This Recalled?
Administration sets leaked at the filter.
Where Was This Sold?
This product was distributed to 6 states: GA, IL, KS, MA, MI, OH
About Zevex Incorporated (dba MOOG Medical Devices Group)
Zevex Incorporated (dba MOOG Medical Devices Group) has 2 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report