---
title: "InfuTronix LLC Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall"
description: "Search InfuTronix LLC recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions."
url: https://isitonrecall.com/brand/infutronix-llc/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Home](https://isitonrecall.com/) / Brand archive

# InfuTronix LLC recall records

**3** reported ongoing

4 records in this archive. Latest source date Mar 20, 2024. 1 published notices do not supply a closure status.

FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## Records and reported status

Mar 20, 2024 FDA company announcement

### [Nimbus: Nimbus Pump System](https://isitonrecall.com/recall/fdapress-16aee4daca36e97c-nimbus-nimbus-pump-system/)

Recall due to a high number (3698) of customer complaints related to the Nimbus Infusion Pump systems

Not supplied Published notice; closure not supplied

Distribution: Not supplied

[Official source for Nimbus: Nimbus Pump System](https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/voluntary-removal-announcement-infutronix-nimbus-ambulatory-infusion-pump-system)

Feb 21, 2024 FDA device enforcement

### [Nimbus Administration Set; Nimbus Flex; Nimbus PainPro (a.k.a. Halo Ambulatory Infusion System); Catalog Number IT1025. Ambulatory Infusion Pump and components](https://isitonrecall.com/recall/fda-device-z-1285-2024-nimbus-administration-set-nimbus-flex-nimbus-painpro-a-k-a-halo-ambulatory-infusion-system-catalog-n/)

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 w...

Class I Reported ongoing

Distribution: Domestic US distribution nationwide. No international distribution.

[Official source for Nimbus Administration Set; Nimbus Flex; Nimbus PainPro (a.k.a. Halo Ambulatory Infusion System); ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1285-2024%22)

Feb 21, 2024 FDA device enforcement

### [Nimbus II Infusion System; Nimbus II PainPRO IT1053; Nimbus II Flex IT1062; Nimbus II Plus IT1078; Nimbus II EpiD IT1124; Nimbus II EMS IT1063; Ambulatory Infusion Pump and comp...](https://isitonrecall.com/recall/fda-device-z-1286-2024-nimbus-ii-infusion-system-nimbus-ii-painpro-it1053-nimbus-ii-flex-it1062-nimbus-ii-plus-it1078-nimbu/)

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 w...

Class I Reported ongoing

Distribution: Domestic US distribution nationwide. No international distribution.

[Official source for Nimbus II Infusion System; Nimbus II PainPRO IT1053; Nimbus II Flex IT1062; Nimbus II Plus IT1078...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1286-2024%22)

Oct 19, 2021 FDA device enforcement

### [Nimbus PainPro Ambulatory Infusion Pumps with software version v4, Model Number IT1072, sold as kit IT1075-DUKE-HSP, IT1076-DUKE-HSP and IT1077-DUKE-HSP](https://isitonrecall.com/recall/fda-device-z-0832-2022-nimbus-painpro-ambulatory-infusion-pumps-with-software-version-v4-model-number-it1072-sold-as-kit-it/)

An unreleased Version 4 Protocol Library was installed on Nimbus PainPro (H) infusion pumps in error that may impact patient safety if used on patients.

Class II Reported ongoing

Distribution: US Nationwide distribution in the states of NC and OH.

[Official source for Nimbus PainPro Ambulatory Infusion Pumps with software version v4, Model Number IT1072, sold as k...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0832-2022%22)

## Reasons in these listed records

- Recall due to a high number (3698) of customer complaints related to the Nimbus Infusion Pump systems
- 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...
- An unreleased Version 4 Protocol Library was installed on Nimbus PainPro (H) infusion pumps in error that may impact patient safety if used on patients.

These examples come from this result page and are not a ranking of every recall reason.

## Checking InfuTronix LLC

### Is there a recall on infutronix llc right now?

This archive contains 4 records, including 3 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product.

### How do I check my package or product?

Compare the product, firm and lot, date, model or serial identifiers with the notice. [Use the label-check guide](https://isitonrecall.com/guides/read-lot-codes/) if you need help locating an identifier.

### Does a matching name mean every item is included?

A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall.

### What if the search finds no matching record?

This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. [Check source coverage](https://isitonrecall.com/sources/) and the agency's current notices.

### Where can I find older records?

Use [monthly archives](https://isitonrecall.com/archives/) or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page.

## Keep checking

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