HUDSON RCI IPN049831Recalls & reported problems
Teleflex Incorporated · NEBULIZER W/TEE & TUBING, SMALL VOLUME I · Class 2
All models of HUDSON RCI (152)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 14026704661517), received between Mar 19, 2021 and Mar 19, 2021 — classified as 1 injury.
The most frequently reported specific device problem is “Use of Device Problem” (1 report).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Most reported problems
Device problems
- Use of Device Problem1
Patient problems
- Insufficient Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMar 19, 2021Use of Device Problem; Use of Device Problem
IT WAS REPORTED THAT "WE USED TO USE THE NEBULIZER REF 41745 IN (B)(6) 2020. WE HAVE REPLACED THIS REF 41745 BY THE REFERENCE 41891. THE SALES REPRESENTATIVE INFORMED ME THAT THE REF 41891 HAD NO AUTO-OCCLUSIVE VALVE. I PROVIDED THIS INFORMATION TO THE HEAD OF THE RESUSCITATION DEPARTMENT. DESPITE THE FACT THAT EVERYONE IS DOING HIS BEST TO PROVIDE ALL THE INFORMATION TO THE OTHERS, WE FACED AN ISSUE WITH A PATIENT WHO WAS IN THE RESUSCITATION DEPARTMENT BECAUSE THE NURSE WAS NOT ENOUGH AWARE OF HOW TO USE THE DEVICE. THE PATIENT "DEPRESSURIZED" BECAUSE OF THIS IGNORANCE WHILST CHANGING THE SMALL RESERVOIR, SO THE CIRCUIT OPENED AND WE PROVIDED RESUSCITATION TO THE PATIENT". IT IS UNKNOWN THE TYPE OF INTERVENTION USED ON PATIENT. PATIENT CONDITION REPORTED AS "FINE".
Patient problems: Insufficient Information
MAUDE report 11528203 ↗
Other NEBULIZER (DIRECT PATIENT INTERFACE) devices
- HUDSON RCI IPN049807Teleflex Incorporated · NEBULIZER (DIRECT PATIENT INTERFACE)62 reports
- Circulaire™ 0330Sunmed, LLC · Nebulizer (Direct Patient Interface)1 recall0 reports
- I neb 00Respironics Respiratory Drug Delivery (Uk) Ltd · NEBULIZER (DIRECT PATIENT INTERFACE)3 deaths15 reports
- VixOne 0209Westmed, Inc. · Nebulizer (Direct Patient Interface)13 reports
- HUDSON RCI IPN040620Teleflex Incorporated · NEBULIZER (DIRECT PATIENT INTERFACE)12 reports
- HUDSON RCI IPN049808Teleflex Incorporated · NEBULIZER (DIRECT PATIENT INTERFACE)6 reports
- HUDSON RCI HUD05014Medline Industries, Inc. · Nebulizer (direct patient interface)6 reports
- VixOne 0210Westmed, Inc. · Nebulizer (Direct Patient Interface)5 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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