Reported Dec 9, 2020 · Terminated

CME America T-Syringe Pump - Neofeed - Product Usage: infusion of medications or fluids requiring continuous or…

CME America, 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: CME America, LLC · 14998 W 6th Ave Ste 830 · Golden, CO · 80401-5025

Is this the product you have?

  • CME America T-Syringe
  • Pump - Neofeed - Product Usageinfusion of medications or fluids requiring continuous or intermittent delivery at precisely-controlled infusion rates through clinically acceptable routes of administration, including intravenous, subcutaneous, percutaneous, intra-arterial, epidural, in close proximity to nerves, and into an intra-operative site (soft tissue/body cavity/surgical wound site)
Lot codes and dates
    • Model Neofeed - Part Number(s) 100-109PSL1A
    • 100-109PSLA
    • 100-110PSLA
  • UDI CodesB101100109PSLA0 B101100109SL1A0
  • B101100110PSLA0 Serial Number

    248 of 248 codes

    • 58767
    • 58763
    • 58761
    • 26410
    • 26439
    • 26447
    • 26456
    • 26460
    • 26461
    • 26462
    • 26463
    • 26464
    • 26465
    • 26158
    • 26157
    • 26159
    • 26160
    • 26161
    • 26134
    • 26135
    • 23136
    • 26047
    • 26008
    • 26055
    • 26054
    • 26053
    • 26048
    • 26036
    • 26050
    • 26031
    • 26035
    • 26028
    • 26007
    • 26022
    • 26014
    • 26033
    • 26012
    • 26005
    • 26023
    • 26002
    • 26000
    • 26024
    • 26034
    • 25998
    • 26010
    • 26001
    • 26009
    • 26003
    • 26015
    • 26004
    • 26006
    • 26016
    • 25930
    • 25931
    • 25932
    • 25933
    • 25938
    • 25939
    • 25960
    • 25961
Amount recalled
Total pumps = 4,182 (all models)

This recall covers 6 products

The agency filed one notice per product. You are reading one of them; the other 5 are below.

Where it was sold

Why it was recalled

Multiple reasons: 1) Due to wear and tear of pump motor block mechanism - may cause under infusion situations without the pump alarm being generated. 2) Due to cracks, pump hardware may be damaged by fluid used during the cleaning process.

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.

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Where this came from

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

Read the FDA (openFDA device enforcement) notice

Notice updated Mar 8, 2022 · Data as of Sep 19, 4:56 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.