ICU Medical recalls 10 drop IV sets with potential 15 drops/mL cannula causing under-delivery of critical medication. Affected units may lead to serious health risks if not corrected.
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 sets that might have a 15-drop cannula instead of the correct 10-drop cannula. This could cause under-delivery of critical medication, risking serious health consequences.
The IV set may contain a 15 drops/mL drop cannula instead of the required 10 drops/mL. This leads to under-delivery of medication, which could be critical for patients needing precise dosing.
Healthcare professionals using these IV sets for patient care. Patients receiving critical medication through these sets are at risk of under-delivery.
Check for the model REF: Z2850, 112" (284 cm) 10 Drop Primary set with 2 Clave, 3 Gang 1o2 Manifold, and 3 Clave. The lot number 4172062 is associated with this recall.
Verify the model number and lot number on the product to confirm if it matches the recalled units.
Reach out to ICU Medical directly for guidance on the correct set and any necessary replacements.
The IV set may contain a 15 drops/mL drop cannula instead of the required 10 drops/mL, leading to under-delivery of critical medication.
Check the model and lot number to confirm if it's affected. Contact ICU Medical for guidance on the correct set and replacements.
Yes, under-delivery of critical medication could lead to serious health consequences if the incorrect cannula is used.
We’ve drafted a message you can send ICU Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1918-2020 — ICU Medical ICU Medical Hello, I own a ICU Medical that is covered by recall Z-1918-2020 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.
