Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1122-2014 — Triton FP Infusion Pump, Part Number 400000, packaged in boxes. The Triton Volumetric Infusion Pump is indicated for delivering infusions of medications, as well as providing TPN (Total Parenteral Nutrition) and PCA (Patient Control Analgesia). It is intended for use in hospitals, ambulatory & nu

U.S. FDA — Device Enforcement · United States · 2014-02-17 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1122-2014
Date of alert: 2014-02-17
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: WalkMed Infusion, LLC
Product category: device
Product type: Devices

Reported risk: 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 an incorrect instruction.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

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