Reported Jul 3, 2013 · Terminated

Brand Name: Intermate Infusion Pump. Indicated for the intravenous administration of medications.

Baxter Healthcare Corp.

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: Baxter Healthcare Corp. · Route 120 And Wilson Rd · Round Lake, IL · 60073-9799

Is this the product you have?

  • Brand NameIntermate Infusion Pump. Indicated for the intravenous administration of medications
Lot codes and dates
  • Product Codes
    • 2C1730K
    • 2C1732K
    • 2C1734K
    • 2C1740K
    • 2C1743K
    • 2C1744K
  • Lot Codes

    107 of 107 codes

    • 10F009
    • 10F049
    • 10F053
    • 10F057
    • 10F095
    • 10J006
    • 10J079
    • 10K077
    • 10M067
    • 10F004
    • 10F015
    • 10G016
    • 10G017
    • 10G018
    • 10G019
    • 10G053
    • 10G054
    • 10H007
    • 10H008
    • 10H009
    • 10H049
    • 10H050
    • 10H051
    • 10H079
    • 10H080
    • 10H081
    • 10H108
    • 10J002
    • 10J009
    • 10J011
    • 10J012
    • 10J077
    • 10J078
    • 10J083
    • 10K009
    • 10K010
    • 10K011
    • 10K012
    • 10K014
    • 10K018
    • 10K070
    • 10K071
    • 10K072
    • 10M015
    • 10M061
    • 10M066
    • 10M071
    • 10M073
    • 10M074
    • 10M082
    • 10F010
    • 10F011
    • 10F079
    • 10G021
    • 10G022
    • 10G023
    • 10H010
    • 10H025
    • 10H026
    • 10H047
  • Expiration Date06/30/13
Amount recalled
3,255,096 total

This recall covers 11 products

The agency filed one notice per product. You are reading one of them; the other 10 are below.

Where it was sold

  • Nationwide
  • PR

Why it was recalled

Baxter Healthcare Corporation (Baxter) is issuing an Urgent Product Recall for the products listed above due to an increase in rupture complaints. Baxter has implemented product and process improvements which have substantially improved product quality. Complaint rates for ruptures have since decreased. Baxter wants to ensure that no affected product remains in the field.

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

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Where this came from

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

Read the FDA (openFDA device enforcement) notice

Notice updated Jun 4, 2014 · Data as of Sep 19, 6:53 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.