Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
EnteraLite Infinity Enteral Feeding Pump identified with the following list Recalled by MOOG Medical Devices Group Due to MOOG Medical Devices Group is conducting a voluntary...
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
EnteraLite Infinity Enteral Feeding Pump identified with the following list numbers: INFKIT2 and INFORNG. The device is used with disposable PVC administration tubing sets to provide a means for the volumetric delivery of fluids used in enteral applications. The EnteraLite Infinity enteral feeding pump with disposable PVC administration tubing sets and user accessories provide a means for the volumetric delivery of fluids used in enteral applications.
Quantity: 8,736
Why Was This Recalled?
MOOG Medical Devices Group is conducting a voluntary for a limited set of serial numbers of the EnteraLite Infinity and Infinity Orange Small Volume Enteral Feeding Pumps because certain diodes on the PCB assembly may result in insufficient voltage to a portion of the pump resulting in an error 13 message and shutting the pump down entirely.
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