Reported Mar 12, 2014 · Terminated

Triton FP Infusion Pump, Part Number 400000, packaged in boxes. The Triton Volumetric Infusion Pump is indicated for…

WalkMed Infusion, LLC

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: WalkMed Infusion, LLC · 96 Inverness Drive East, Suite J · Englewood, CO · 80112-5311

Is this the product you have?

  • 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 & nursing home (extended care) settings, and home care environments.
Lot codes and dates
  • 150 of 150 codes

    • PFA14001
    • PFA14002
    • PFA14003
    • PFA14004
    • PFA14005
    • PFA14006
    • PFA14007
    • PFA14008
    • PFA14009
    • PFA14010
    • PFA14011
    • PFA14012
    • PFA14013
    • PFA14014
    • PFA14015
    • PFA14016
    • PFA14017
    • PFA14018
    • PFA14019
    • PFA14020
    • PFA14021
    • PFA14022
    • PFA14023
    • PFA14024
    • PFA14025
    • PFA14026
    • PFA14027
    • PFA14028
    • PFA14029
    • PFA14030
    • PFA14031
    • PFA14032
    • PFA14033
    • PFA14034
    • PFA14035
    • PFA14036
    • PFA14037
    • PFA14038
    • PFA14039
    • PFA14040
    • PFA14041
    • PFA14042
    • PFA14043
    • PFA14044
    • PFA14045
    • PFA14046
    • PFA14047
    • PFA14048
    • PFA14049
    • PFA14050
    • PFA14051
    • PFA14052
    • PFA14053
    • PFA14054
    • PFA14055
    • PFA14056
    • PFA14057
    • PFA14058
    • PFA14059
    • PFA14060
Amount recalled
797

Where it was sold

Why it was recalled

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.

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

Free recall alerts

Get alerted about new WalkMed Infusion, LLC recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Oct 6, 2014 · Data as of Sep 19, 6:01 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.