ICU Medical recalls Plum Duo IV pumps with specific list numbers and software versions due to potential piggyback flush errors that may prevent proper flushing of IV lines.
Plum Solo and Duo Infusion pumps include a feature, that when selected, automatically flushes the downstream line after a piggyback therapy. The programmed flush volume is delivered from the primary line container at the piggyback therapy rate after the piggyback therapy is complete. In certain cases, as described below, the clinician may receive an Upper Hard Limit (UHL) or Lower Hard Limit (LHL) Violation message when programming a piggyback flush, which prevents the flush from being programmed.
ICU Medical is recalling certain Plum Duo Precision IV pumps that may not flush IV lines properly after piggyback therapy, which could lead to incorrect medication delivery. This issue affects specific model numbers and software versions sold in the US and Philippines.
The pump's piggyback flush feature may not activate correctly, causing the system to show an error message that prevents the flush from being programmed. This could lead to improper medication delivery if the IV line isn't flushed properly after piggyback therapy.
Healthcare professionals using ICU Medical Plum Duo IV pumps with list numbers 400020403 (US) or 400021003 (Philippines) and software versions 1.2.2 or 1.2.0 are most at risk. Patients receiving IV treatments through these pumps may be affected if the flush fails to occur.
Check for list numbers 400020403 (US) or 400021003 (Philippines) and software versions 1.2.2 (US) or 1.2.0 (Philippines) on the pump's label or documentation.
Verify the software version on the pump to ensure it is not 1.2.2 for US models or 1.2.0 for Philippine models.
The pump may not flush IV lines properly after piggyback therapy, which can cause errors in medication delivery.
US models with software version 1.2.2 and Philippine models with software version 1.2.0.
Check the pump's label for list numbers 400020403 (US) or 400021003 (Philippines) and software versions 1.2.2 or 1.2.0.
We’ve drafted a message you can send ICU Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1119-2026 — ICU Medical ICU Medical Hello, I own a ICU Medical that is covered by recall Z-1119-2026 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.
