HUDSON RCI COMFORT FLO Humidification System
Medical device recall Z-1114-2020. Published in FDA’s Enforcement Report on Feb 19, 2020.
- FDA Class I
No Watch here, and no alerts: openFDA asks that its enforcement data “should not be used as a method to collect data to issue alerts to the public, nor should it be used to track the lifecycle of a recall” (openFDA). For FDA’s own recall emails, subscribe at FDA. FDA’s own record is on accessdata.fda.gov.
The short answer
Published in FDA’s Enforcement Report on Feb 19, 2020. Copied from openFDA on Oct 20, 2026.
- Class I FDA’s most serious class (needs attention)
- Terminated its status, in FDA’s file
- Nationwide FDA’s word for where it went
- 127293 devices how much, in FDA’s words
Every line below is in FDA’s own words, with its source beside it. FDA’s terms are explained in FDA’s own words.
How serious is it, by FDA’s class?
Class I, the most serious of FDA’s three classes.
“Dangerous or defective products that predictably could cause serious health problems or death. Examples include: food found to contain botulinum toxin, food with undeclared allergens, a label mix-up on a lifesaving drug, or a defective artificial heart valve.”
openFDA, in plain words, its enforcement report fields.
“Class I is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.”
FDA’s rule, 21 CFR 7.3(m)(1), eCFR.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
What’s wrong with it?
There is the potential for water to flood the column and enter the circuit under circumstances where an abnormal pressure differential is created between the water bottle and the column during high flow oxygen therapy.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Which ones are recalled?
HUDSON RCI COMFORT FLO Humidification System, REF 2410, humidifier nebulizer kit
127293 devices, in FDA’s words.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Codes to check against yours
GTIN 14026704659347 Lot Numbers: 74M1400306 74M1400711 74M1401528 74B1500017 74C1501165 74C1502056 74D1500014 74D1500695 74D1501704 74D1501219 74D1501910 74E1500306 74E1501372 74E1501373 74E1501374 74E1501375 74E1501371 74M1500846…
Every code shown here, 1,209 characters
GTIN 14026704659347 Lot Numbers: 74M1400306 74M1400711 74M1401528 74B1500017 74C1501165 74C1502056 74D1500014 74D1500695 74D1501704 74D1501219 74D1501910 74E1500306 74E1501372 74E1501373 74E1501374 74E1501375 74E1501371 74M1500846 74M1501089 74A1600595 74A1601230 74B1600045 74C1601038 74C1601644 74C1602406 74C1601594 74C1602113 74C1602114 74C1602115 74C1602116 74C1602117 74C1602146 74D1600254 74D1600253 74D1601801 74E1600052 74E1601253 74F1600669 74F1603321 74G1600071 74G1601038 74H1600051 74H1600052 74H1603043 74J1601205 74J1601478 74J1602063 74J1602658 74J1602865 74J1602864 74K1602260 74K1602874 74L1600133 74L1601767 74L1602602 74M1600527 74M1601523 74A1700288 74A1700995 74A1701895 74B1701971 74B1702316 74C1701847 74D1700109 74D1701791 74E1700933 74E1702182 74E1702251 74F1700030 74F1702959 74G1700802 74H1700006 74H1700404 74J1700408 74J1701883 74J1701884 74K1700025 74K1700305 74L1700955 74L1701845 74M1700483 74A1801553 74B1801391 74C1802117 74C1802118 74D1800085 74D1801077 74E1800628 74E1800789 74E1802236 74F1800042 74E1803151 74F1801157 74G1800356 74H1800881 74H1802700 74K1800753 74L1802033 74M1800649 74A1900149 74A1901354 74A1901414 74B1900011 74B1900245 74B1902467 74D1901101 74D1903025
Copied exactly as FDA lists them: lot and serial numbers, dates and other codes on the product or its label.
Where did it go?
FDA’s words for the “general area of initial distribution”: where the firm first shipped it.
nationwide
These words name no state.
What FDA means by nationwide
“The term “nationwide” is defined to mean the fifty states or a significant portion. Note that subsequent distribution by the consignees to other parties may not be included.”
openFDA, its enforcement report fields.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
Is it still going on?
Terminated, in FDA’s file.
“FDA has determined that all reasonable efforts have been made to remove or correct the violative product in accordance with the recall strategy, and proper disposition has been made according to the degree of hazard.”
openFDA, on “Terminated”, its enforcement report fields.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
- The firm began the recall on Dec 13, 2019.
- FDA classified it on Feb 7, 2020.
- FDA’s Enforcement Report published it on Feb 19, 2020.
- FDA terminated it on Apr 30, 2024.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Who is recalling it?
- TELEFLEX MEDICAL INC, of Morrisville, NC.
- Who began it, in FDA’s words: Voluntary: Firm initiated.
- How the firm first told its customers: Letter.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
What this record can’t tell you
- Whether your own one is affected: compare the codes, dates and numbers above with yours. When unsure, ask the firm or the store.
- Where it went after the firm’s first shipments. FDA’s words cover the firm’s initial distribution, and, in FDA’s words, “subsequent distribution by the consignees to other parties may not be included.”
- How many have been returned, corrected or destroyed: FDA’s report doesn’t say.
- Whether anyone was hurt or fell ill: the report doesn’t say.
- How current it is: openFDA publishes FDA’s Enforcement Report weekly, after FDA does, and a firm can announce a recall weeks before it appears there. openFDA’s own caution: “This data should not be used as a method to collect data to issue alerts to the public, nor should it be used to track the lifecycle of a recall.”
- A product with no recall here isn’t safe by that: FDA’s report lists the recalls FDA classified, and when.
Hearth Record wrote these lines; the quotations are FDA’s.
Sources
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U.S. Food and Drug Administration, Device recall enforcement reports.
Released Oct 14, 2026 and checked Oct 20, 2026. Updated weekly. Public domain (CC0 1.0, openFDA). FDA asks that nothing suggest it endorses this site.
Recalls of food, medicines, medical devices, pet food and animal drugs are from the U.S. Food and Drug Administration (FDA). FDA does not endorse Hearth Record. openFDA: “Do not rely on openFDA to make decisions regarding medical care.” Copied on Oct 20, 2026.