---
title: "Medline, Teleflex: Hudson RCI Neonatal/Infant Heated Wire Breathing Circuits — FDA announcement Aug 6, 2026 | Is It on Recall"
description: "Due to heated wire connector (pigtail) at the Neptune humidifier may exhibit discoloration, melting, smoke, burning odor, or other signs of localized thermal da"
url: https://isitonrecall.com/recall/fdapress-1c8bd6cdabe7c66e-medline-teleflex-hudson-rci-neonatal-infant-heated-wire-breathing-circuits/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA company announcement

# Medline, Teleflex: Hudson RCI Neonatal/Infant Heated Wire Breathing Circuits — FDA announcement Aug 6, 2026

Published notice; closure not supplied

A company announcement posted by FDA. The listing date can differ from the original announcement date. The absence of a termination marker does not prove the recall is currently ongoing.

Source date Aug 6, 2026. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

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/).

## What the record says

- **Product**: Hudson RCI Neonatal/Infant Heated Wire Breathing Circuits
- **Reason**: Due to heated wire connector (pigtail) at the Neptune humidifier may exhibit discoloration, melting, smoke, burning odor, or other signs of localized thermal damage
- **Classification**: Not supplied
- **Recalling firm**: Medline Industries, LP
- **Quantity**: Not supplied
- **Agency-reported status**: Company recall announcement
- **Source record identifier**: 1c8bd6cdabe7c66e

[Open the official record](https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/medline-industries-lp-issues-nationwide-recall-hudson-rci-neonatalinfant-heated-wire-breathing)

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | Medline Item Number \| Teleflex Item Number; HUD78001KIT \| 780-01KIT; HUD78007 \| 780-07; HUD78007KIT \| 780-07KIT; HUD78008KIT \| 780-08KIT; HUD78009 \| 780-09; HUD78009KIT \| 780-09KIT; HUD78013 \| 780-13; HUD78014 \| 780-14; HUD78015 \| 780-15; HUD78017KIT \| 780-17KIT; HUD78018 \| 780-18; HUD78018KIT \| 780-18KIT; HUD78019 \| 780-19; HUD88001KIT \| 880-01KIT; HUD88013KIT \| 880-13KIT; HUD88014KIT \| 880-14KIT; HUD88015KIT \| 880-15KIT; HUD88017KIT \| 880-17KIT |

Match all identifying details in the current notice. A brand name alone is not enough.

## Product tables from the announcement

These identifying details come from the company announcement posted by FDA. Check the current notice for revisions.

**FDA company announcement, table 1**

| Medline Item Number | Teleflex Item Number |
| --- | --- |
| HUD78001KIT | 780-01KIT |
| HUD78007 | 780-07 |
| HUD78007KIT | 780-07KIT |
| HUD78008KIT | 780-08KIT |
| HUD78009 | 780-09 |
| HUD78009KIT | 780-09KIT |
| HUD78013 | 780-13 |
| HUD78014 | 780-14 |
| HUD78015 | 780-15 |
| HUD78017KIT | 780-17KIT |
| HUD78018 | 780-18 |
| HUD78018KIT | 780-18KIT |
| HUD78019 | 780-19 |
| HUD88001KIT | 880-01KIT |
| HUD88013KIT | 880-13KIT |
| HUD88014KIT | 880-14KIT |
| HUD88015KIT | 880-15KIT |
| HUD88017KIT | 880-17KIT |

Announcement retrieved Oct 1, 2026. [Official announcement](https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/medline-industries-lp-issues-nationwide-recall-hudson-rci-neonatalinfant-heated-wire-breathing).

## Distribution

Not supplied

No US distribution state could be established from this record. Check the official notice.

## Dates in the source

- **Fda listing date**: Aug 6, 2026
- **Company announcement date**: Aug 5, 2026

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Consumers who have the affected Hudson RCI Neonatal/Infant Heated Wire Breathing Circuits should stop using and discard the device. Consumers should not return product to Medline. Consumers with questions regarding this recall can contact Medline by phone at 866-359-1704 Monday through Friday between the hours of 8am and 5pm CST or recalls@medline.com. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to using this medical device.

[Read the current instructions](https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/medline-industries-lp-issues-nationwide-recall-hudson-rci-neonatalinfant-heated-wire-breathing)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Medline Industries, LP records](https://isitonrecall.com/brand/medline-industries-lp/)