Product Recall: WalkMed Infusion Recalls Triton & Triton fp

WalkMed Infusion has issued a Medical Device Recall for the Triton and Triton fp infusion pumps (model numbers 300000 and 400000) effective immediately. It is recommended that pumps be inspected to determine if they are model number 300000 or 400000. If you have affected pumps, contact Right Way Medical to discuss your options.

WalkMed Infusion recommends that users stop use of and replace the Triton and Triton fp infusion pumps with alternative devices as soon as possible. To minimize patient disruption, WalkMed will continue to provide IV administration sets, provide preventive maintenance and service for distributed pumps, and make available any parts necessary for the repair or service of units for up to 3 months from June 14th.

WalkMed Infusion has also issued a recall of Triton and Triton fp administration sets (see product type and lot numbers affected below) due to the potential presence of particulate in or on the Administration Sets. If particulate in the Administration Sets is administered intravenously, it may result in local inflammation, mechanical disruption of tissue or immune response to the particulate. Affected lot numbers may be exchanged for new sets that have passed inspection for particulate.