ICU Medical recalls 10-drop IV admin sets with potential 15-drop cannula causing under-delivery of medication. Affected units may lead to serious health risks if critical drugs are not delivered properly.
There is a potential that IV administration sets contain a 15 drops/mL drop cannula instead of a 10 drops/mL drop cannula within the drip chamber. An infusion set with an incorrect drop cannula could result in inaccurate delivery of the intended infusion volume (under-delivery). This could result in under-delivery of critical medication which may lead to serious adverse health consequences.
ICU Medical is recalling 10-drop IV administration sets that might have a 15-drop cannula instead of the correct 10-drop cannula. This could cause under-delivery of critical medications, risking serious health consequences.
The IV set might have a 15-drop cannula instead of the required 10-drop cannula. This causes the set to deliver less medication than intended, potentially leading to under-delivery of critical drugs. Under-delivery of critical medications could result in serious health consequences.
Healthcare professionals using these IV sets for patient medication administration are most at risk. Patients receiving critical medications through these sets could experience under-delivery.
Check for the model: REF B9900-287, 82" (208 cm) Appx 10.4 ml, 10 Drop Admin Set with Pre-Slit Port, Clave, 1 Ext, Rotating Luer, Sterile R. Units sold with UDI: (01)00887709016842 and Lot number 4167007 are affected.
Verify the model number and lot number on the product label to confirm if it matches the recalled units.
Reach out to ICU Medical for guidance on next steps if you have the recalled set.
The recall is due to a potential 15-drop cannula in some sets instead of the required 10-drop cannula, which could cause under-delivery of critical medications.
Check the model and lot number to see if it matches the recalled units. Contact ICU Medical for further instructions.
Yes, under-delivery of critical medications could lead to serious health consequences if the set is used incorrectly.
We’ve drafted a message you can send ICU Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1914-2020 — ICU Medical ICU Medical Hello, I own a ICU Medical that is covered by recall Z-1914-2020 from ICU Medical. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
