HUDSON RCI IPN049730Recalls & reported problems
Teleflex Incorporated · Adult Softech Plus Nasal Cannula W/7ft(2.1m) Green Star Lumen Tubing · Class 1
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
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 14026704625243), received between Sep 26, 2021 and Sep 26, 2021 — classified as 1 malfunction.
The most frequently reported specific device problem is “Material Too Soft/Flexible” (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
- Material Too Soft/Flexible1
Patient problems
- Unspecified Respiratory Problem1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 26, 2021Material Too Soft/Flexible; Material Too Soft/Flexible
IT WAS REPORTED THAT:" HUDSON RCI ADULT SOFTECH PLUS NASAL CANNULA. THESE DON'T SEEM TO BE FITTING THE PATIENTS WELL. THEY WON'T STAY IN PLACE DESPITE WHICH WAY THEY ARE PLACED. THIS THEN BECOMES UNCOMFORTABLE FOR THE PATIENT AND REDUCES THE THERAPEUTIC SIGNIFICANCE". NO PATIENT HARM OR INJURY REPORTED. DEVICE WAS EXCHANGED FOR AN OXYGEN MASK. PATIENT CONDITION REPORTED AS "FINE".
Patient problems: Unspecified Respiratory Problem
MAUDE report 12531150 ↗
Other CANNULA, NASAL, OXYGEN devices
- Fisher & Paykel Healthcare OPT844Fisher & Paykel Healthcare Limited · Cannula, Nasal, Oxygen39 reports
- Fisher and Paykel Healthcare OPT312Fisher & Paykel Healthcare Limited · Cannula, Nasal, Oxygen22 reports
- Fisher and Paykel Healthcare OPT314Fisher & Paykel Healthcare Limited · Cannula, Nasal, Oxygen17 reports
- O2 Cannula 001366Salter Labs · Cannula, Nasal, Oxygen10 reports
- O2 Cannula 001365Salter Labs · Cannula, Nasal, Oxygen9 reports
- N/A 16SOFT-4Salter Labs · CANNULA, NASAL, OXYGEN8 reports
- N/A 1053-7Salter Labs · CANNULA, NASAL, OXYGEN8 reports
- Fisher & Paykel Healthcare OPT842Fisher & Paykel Healthcare Limited · Cannula, Nasal, Oxygen7 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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