InfuTronix recalls Nimbus Administration Set, Nimbus Flex, and Nimbus PainPro infusion pumps due to potential battery failure, system errors, and drug leakage risks. All units with catalog number IT1025 are affected and will no longer be available after June 20, 2024.
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 Nimbus Administration Set, Nimbus Flex, and Nimbus PainPro infusion pumps because they can fail in multiple ways, including battery issues, system errors, and drug leakage. This poses a risk of serious injury or death if the device malfunctions during use.
The pumps can fail due to battery issues, system errors, or leaks, which may lead to incorrect drug delivery, device damage, or serious injury. These failures could occur during normal use without warning.
Patients using these infusion pumps for medical treatments are most at risk. Anyone with the recalled catalog number IT1025 should stop using the device immediately.
Check for the catalog number IT1025 on the pump or its packaging. The recalled models include Nimbus Administration Set, Nimbus Flex, and Nimbus PainPro (also known as Halo Ambulatory Infusion System).
Immediately stop using the Nimbus Administration Set, Nimbus Flex, or Nimbus PainPro pumps if you have the catalog number IT1025.
Nimbus Administration Set, Nimbus Flex, and Nimbus PainPro (also known as Halo Ambulatory Infusion System) with catalog number IT1025.
InfuTronix is removing these pumps from the market due to multiple potential failure modes, including battery failure, system errors, and drug leakage risks.
The devices will no longer be available or supported after June 20, 2024.
We’ve drafted a message you can send InfuTronix to request your refund or repair — edit it as you like.
Subject: Recall Z-1285-2024 — InfuTronix InfuTronix Hello, I own a InfuTronix that is covered by recall Z-1285-2024 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.
