ICU Medical recalls veterinary IV sets with potential 15 drops/mL cannula causing under-delivery of critical medication. Affected units sold outside US; no remedy stated.
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 recalls veterinary IV administration sets that might deliver less medication than intended. This could cause serious health issues if critical drugs aren't properly administered.
The sets may contain a 15 drops/mL cannula instead of the required 10 drops/mL. This causes under-delivery of medication, potentially leading to serious health consequences if critical drugs are administered.
Veterinary professionals using the recalled sets in the US. The risk is highest for animals receiving critical medications through these sets.
Check for the model number AH7117 111" 10 Drop Admin Set with lot number 4173657. These sets were sold outside the US and not distributed within the US.
Look for the model number AH7117 111" 10 Drop Admin Set and lot number 4173657 on the packaging.
No, the product was not distributed within the US.
The sets may deliver less medication than intended, which could cause serious health issues for animals receiving critical medications.
The recall record does not state any remedy.
We’ve drafted a message you can send ICU Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1911-2020 — ICU Medical ICU Medical Hello, I own a ICU Medical that is covered by recall Z-1911-2020 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.
