Recall archive
3 recalls · page 1 of 1
Reported Jul 27, 2016
The pump (with cushioning foam inserts) is packaged in a single pump box. Four pump boxes are placed in an over-shipper…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.WalkMed Infusion, LLC
Matched: Brand · Reason for recall — WalkMed Infusion, LLC Announces a Voluntary Field Action of the Triton Infusion Pump (model 300000) and Triton FP Infusion Pump (model 400000) Due to…
16 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 18, 2015
Triton Infusion Pump (model 300000) and Triton fp Infusion Pump (model 400000) (proprietary name: AFF (Mark I)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.WalkMed Infusion, LLC
Matched: Brand · Product · Product details · Reason for recall — 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…
FDA (openFDA device enforcement)
Reported Mar 12, 2014
Triton FP Infusion Pump, Part Number 400000, packaged in boxes. The Triton Volumetric Infusion Pump is indicated for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.WalkMed Infusion, LLC
Matched: Brand · Product · Product details · Reason for recall — WalkMed Infusion is initiaing a recall on their Triton FP Infusion Pump, Part Number 400000 due to the label on the right side of the pump containing…
FDA (openFDA device enforcement)
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