Reported Oct 28, 2020 · Terminated

142 IN (361cm) APPX 18.8 ml, 15 DROP SET 4 MicroClave CLEAR, REMV 3-PORT NanoClave w/ BCV. 1 unit per pouch, 25 pouches…

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. · 951 Calle Amanecer · San Clemente, CA · 92673-6212

Is this the product you have?

6 of 6 products

Products covered by this recall
#BarcodesProduct as published
110887709089393142 IN (361cm) APPX 18.8 ml, 15 DROP SET 4 MicroClave CLEAR, REMV 3-PORT NanoClave w/ BCV. 1 unit per pouch, 25 pouches per case. UDI:(01)10887709089393(17)250101(30)25(10)4573948
210887709089393(01)10887709089393(17)250101(30)25(10)4603380
310887709089393(01)10887709089393(17)250101(30)25(10)4711169
410887709089393(01)10887709089393(17)241201(30)25(10)4493653
510887709089393(01)10887709089393(17)241201(30)25(10)4536737
610887709089393(01)10887709089393(17)250201(30)25(10)4733710. The Intravascular Administration Set is a single use, sterile, non-pyrogenic device which provides access for the administration of fluids from a container to a patient's vascular system through the administration set's needle or catheter (which is inserted into a vein).
Lot codes and dates
  • Lot Numbers
    • 4573948
    • 4603380
    • 4711169
    • 4493653
    • 4536737 4733710
Amount recalled
Total of all products (Listed #1 thru 101) = 304735 units

This recall covers 99 products

The agency filed one notice per product. You are reading one of them; the other 98 are below.

86 more are in the archive.

Where it was sold

Why it was recalled

Identification of a potential manufacturing defect on the internal surface of the NanoClave within specific lots of NanoClave sets, which may inhibit a proper seal with the NanoClave spike.

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 May 11, 2023 · Data as of Sep 19, 5:41 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.