Reported Sep 23, 2026 · Ongoing · Updated Sep 29, 2026

CADD Yellow Medication Cassette Reservoir with NRFit connector US Product Codes: 21-7600-24, 21-7609-24 OUS Product…

ICU Medical, Inc.

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: ICU Medical, Inc. · 600 N Field Dr · Lake Forest, IL · 60045-4835

Is this the product you have?

  • CADD Yellow Medication Cassette Reservoir
  • with NRFit connector US Product Codes
    • 21-7600-24
    • 21-7609-24
  • OUS Product Codes
    • 21-7609-24
    • 21-7600-24
    • 21-7600-24
    • 21-7600-24
    • 21-7609-24
    • 21-7609-24
    • 21-7600-24
    • 21-7600-24
    • 21-7609-24
    • 21-7609-24
    • 21-7600-24
    • 21-7600-24
    • 21-7609-24
    • 21-7600-24
    • 21-7600-24
    • 21-7609-24
    • 21-7609-24JP
    • 21-7600-24JP
    • 21-7609-24
    • 21-7609-24
    • 21-7600-24
    • 21-7600-24
    • 21-7609-24
    • 21-7600-24
    • 21-7600-24
    • 21-7600-24
    • 21-7609-24
Lot codes and dates
  • 21-7600-24 UDI-DI 30610586044001 Lots
    • 6026878
    • 6037784
    • 6054015
    • 6062724
    • 6070616
    • 6082332
    • 6092886
    • 6101906
    • 6108556
    • 6126029
    • 6140893
    • 6143454
    • 6147696
    • 6147697
    • 6162769
    • 6155095
    • 6166032
    • 6171587
    • 6171586
    • 21-7609-24
    UDI-DI 30610586044018 Lot
    • 6022079
    • 6037697
    • 6037698
    • 6053978
    • 6061525
    • 6072970
    • 6072964
    • 6070575
    • 6077773
    • 6092846
    • 6101798
    • 6108514
    • 6108515
    • 6108516
    • 6140862
    • 6140861
    • 6140865
    • 6155132
Amount recalled
185,688 units

This recall covers 9 products

The agency filed one notice per product. You are reading one of them; the other 8 are below.

Where it was sold

Why it was recalled

Reservoirs may exhibit medication leakage at the joint between luer connector and tubing. Issue could result in delay or interruption of therapy, under delivery of medication, exposure to infectious or toxic agents, or air embolus.

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

Data as of Nov 4, 1:01 AM 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.