Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Triton Infusion Pump (model 300000) and Triton fp Infusion Pump Recalled by WalkMed Infusion, LLC Due to The device might fail to detect air in...
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 WalkMed Infusion, LLC directly.
Affected Products
Triton Infusion Pump (model 300000) and Triton fp Infusion Pump (model 400000) (proprietary name: AFF (Mark I) Volumetric Infusion Pump). Used to pump fluids into a patient in a controlled manner.
Quantity: 4695 units
Why Was This Recalled?
The device might fail to detect air in line while infusing the medication Venofer. This may occur when a drop of Venofer gets stuck in the tubing adjacent to the bubble detector and the Total Volume Limit is programmed higher than the actual bag volume.
Where Was This Sold?
This product was distributed to 22 states: AL, CA, CO, DE, FL, GA, IL, MD, MA, MI, MN, MS, NV, NJ, NM, NY, NC, OH, PA, TN, TX, WA
About WalkMed Infusion, LLC
WalkMed Infusion, LLC has 19 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report