Reported Sep 2, 2026 · Ongoing · Updated Sep 16, 2026

Medline breathing circuits labeled as

Medline Industries, LP

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Medline Industries, LP · 3 Lakes Dr · Northfield, IL · 60093-2753

Is this the product you have?

Medline breathing circuits labeled as

6 of 6 products

Products covered by this recall
Model / numberProduct as published
780-07HUDSON RCI, CIRCUIT, HTD, DL, NEONATE, 48, Medline Product Number/SKU HUD78007 (Teleflex Product Number/ )
780-09HUDSON RCI, DBM-CIRCUIT,VENT,NEONATAL,21 V, Medline Product Number/SKU HUD78009 (Teleflex Product Number/ )
780-13HUDSON RCI, DBD-CIRCUIT,VENT,INSIRATORY,HEATED,NEO,4, Medline Product Number/ (Teleflex Product Number/SKU 780-13)
780-14HUDSON RCI, DBD-CIRCUIT,VENT,INSIRATORY,HEATED,NEO,4, Medline Product Number/ (Teleflex Product Number/SKU 780-14)
780-15HUDSON RCI, DBD-CIRCUIT, HTD, DUAL LIMB, NEONATE, Medline Product Number/ (Teleflex Product Number/SKU 780-15)
780-18HUDSON RCI, CIRCUIT,NEO,DUAL,WIRE,60 IN, Medline Product Number/SKU HUD78018) (Teleflex Product Number/ ).
Lot codes and dates

6 of 6 products

Products covered by this recall
Model / numberBarcodesProduct as published
HUD780071019734404246320197344042460Medline Product Number/ , UDI/DI 10197344042463 (each) 20197344042460 (case), All lot numbers
HUD78009Medline Product Number/ , UDI/DI Discontinued (each) Discontinued (case), All lot numbers
780-13Medline Product Number/ , UDI/DI Discontinued (each) Discontinued (case), All lot numbers
780-14Medline Product Number/ , UDI/DI Discontinued (each) Discontinued (case), All lot numbers
780-15Medline Product Number/ , UDI/DI Discontinued (each) Discontinued (case), All lot numbers
HUD780181019734401066020197344010667Medline Product Number/ , UDI/DI 10197344010660 (each) 20197344010667 (case), All lot numbers.
Amount recalled
145525 units

This recall covers 19 products

The agency filed one notice per product. You are reading one of them; the other 18 are below.

6 more are in the archive.

Where it was sold

  • Nationwide

Why it was recalled

Neonatal and infant heated wire breathing circuits may experience sporadic failure. The heated wire connector (pigtail) at the humidifier may exhibit discoloration, melting, smoke, burning odor, or other signs of localized thermal damage. Device failure may predispose infant to bronchospasm, inspissated secretions, and airway obstruction, as well as inadvertent positive end-expiratory pressure (PEEP), circuit obstruction, or accidental lavage of pooled fluid into the airway, elevated oxygen consumption, and worsening respiratory distress.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (Enforcement Report)

Read the FDA (weekly enforcement report) notice

Notice updated Sep 14, 2026 · Data as of Sep 19, 3:39 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.