ICU Medical recalls 100" 10 Drop Admin Sets with incorrect drop cannulas that may cause under-delivery of critical medication. Affected units have specific lot numbers and purple color. Contact for remedy.
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 100" 10 Drop Admin Sets that may have a 15 drops/mL drop cannula instead of the required 10 drops/mL. This could lead to under-delivery of critical medication, risking serious health consequences.
The sets might contain a 15 drops/mL drop cannula instead of the required 10 drops/mL. This error causes the IV to deliver less medication than intended, potentially leading to under-delivery of critical treatments.
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 purple color and lot numbers 4172061 or 4173149 on the product label. The product is identified by the reference number Z2560 and includes a hand pump and rotating Luer connector.
Check the product label for the purple color and lot numbers 4172061 or 4173149.
The sets may contain a 15 drops/mL drop cannula instead of the required 10 drops/mL, which could cause under-delivery of critical medication.
Look for the purple color and lot numbers 4172061 or 4173149 on the product label.
The recall record does not specify a remedy, so contact ICU Medical directly for guidance.
We’ve drafted a message you can send ICU Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1916-2020 — ICU Medical ICU Medical Hello, I own a ICU Medical that is covered by recall Z-1916-2020 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.
