InfuTronix recalls Nimbus II infusion pumps due to battery failures, system errors, and drug leaks. All units sold before June 20, 2024, are affected. Stop using immediately to avoid serious injury risks.
InfuTronix is removing the Nimbus Infusion Pump Systems from the market due to multiple potential failure modes, including battery failure, upstream occlusion, system errors, drug product leakage, high or low flow rate, or damaged pump housing. The device will not be available or supported after June 20, 2024.
InfuTronix is recalling multiple Nimbus II infusion pump models because they can fail in ways that might cause serious injury, like battery issues, drug leaks, or incorrect flow rates. These pumps will no longer be available or supported after June 20, 2024.
The pumps can fail due to battery issues, blockages, system errors, or leaks of medication. This could lead to incorrect dosing, serious injury, or even death if the device stops working unexpectedly during treatment.
People using any Nimbus II infusion pump models listed in the recall, including PainPRO, Flex, Plus, EpiD, and EMS versions, are affected. Those with medical conditions requiring continuous infusion therapy are at highest risk.
Check for the model names: Nimbus II PainPRO IT1053, Flex IT1062, Plus IT1078, EpiD, or EMS. The recall includes all units sold before June 20, 2024, with specific lot numbers listed in the official notice.
Discontinue use of the Nimbus II infusion pump system as it poses serious injury risks.
Yes, all Nimbus II infusion pump models (PainPRO, Flex, Plus, EpiD, EMS) sold before June 20, 2024, are included in this recall.
Check the model name and lot number on your pump. The recall includes specific models like Nimbus II PainPRO IT1053 and lots such as AHZ081-190619096.
Stop using it immediately and contact InfuTronix for instructions on disposal or replacement.
We’ve drafted a message you can send InfuTronix to request your refund or repair — edit it as you like.
Subject: Recall Z-1286-2024 — InfuTronix InfuTronix Hello, I own a InfuTronix that is covered by recall Z-1286-2024 from InfuTronix. 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.
