Reported Oct 30, 2024 · Ongoing

CADD Medication Cassette Reservoir, 100mL, FS, YELLOW, Product Code 21-7300-24

Smiths Medical ASD 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: Smiths Medical ASD Inc. · 6000 Nathan Ln N · Minneapolis, MN · 55442-1690

Is this the product you have?

  • CADD Medication Cassette Reservoir, 100mL, FS, YELLOW, Product Code 21-7300-24
Lot codes and dates
  • UDI/DI 10610586027192
  • Lot Numbers
    • 3971732
    • 3971731
    • 4034016
    • 3977457
    • 4013365
    • 4019421
    • 4019422
    • 4034015
    • 4037744
    • 4037745
    • 4034018
    • 4034017
    • 4046844
    • 4046843
    • 4053912
    • 4048899
Amount recalled
26160 units

This recall covers 14 products

The agency filed one notice per product. You are reading one of them; the other 13 are below.

1 more are in the archive.

Why it was recalled

Certain CADD Medication Cassette Reservoirs may exhibit a weakened weld joint between the medication bag and tubing due to a production equipment malfunction. This could result in a medication leakage.

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 Sep 19, 6:22 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.