Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
***This recall is being conducted due to an incomplete recall Recalled by MOOG Medical Devices Group Due to This recall is the same issue for the...
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 MOOG Medical Devices Group directly.
Affected Products
***This recall is being conducted due to an incomplete recall for RES 57829*** Curlin Infusion Administration Set, REF 340-4165, Sterile EO, The Curlin Ambulatory Infusion Pump System with disposable PVC Administration Tubing Sets and user accessories, provide a means for the volumetric delivery of fluids used in Parenteral, Enteral, Epidural, Subcutaneous and Intravenous applications.
Quantity: 12,000 sets
Why Was This Recalled?
This recall is the same issue for the FDA processed recall initiated by Moog Medical Devices on 1/25/11 which was related to customers reporting unclearable Air-In-Line alarm with specific lot numbers of Curlin Administration Sets used with Curlin Ambulatory Infusion Pumps. The lots associated with this recall were inadvertently omitted from the original recall which has since been terminated by
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About MOOG Medical Devices Group
MOOG Medical Devices Group has 5 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report