WalkMed Infusion, LLC Recall: Triton Infusion Pump (model 300000) and Triton fp Infusion P
WalkMed Infusion, LLC Recall: Triton Infusion Pump (model 300000) and Triton fp Infusion P is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: WalkMed Infusion, LLC; Product: Triton Infusion Pump (model 300000) and Triton fp Infusion Pump (model 400000) (proprietary name: AFF (Mark I) Volu
| Recalling firm | WalkMed Infusion, LLC |
|---|---|
| Product | 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. |
| 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 adjacent to the bubble detector and the Total Volume Limit is programmed higher than the actual bag volume. |
| Classification | Class II (moderate — may cause temporary or reversible health consequences) |
| Status | Terminated |
| Distribution | Distributed in the states of AL, CA, CO, DE, FL, GA, IL, MA, MD, MI, MN, MS, NC, NJ, NM, NV, NY, OH, PA, TN, TX, and WA. |
| Recall initiated | 20151001 |
| Recall number | Z-0242-2016 |
| Category | device |
| State | CO |
| Country | United States |
$29/mo
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