HUDSON RCI IPN913797Recalls & reported problems
Teleflex Incorporated · Breathing Circuit (10mm) · 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 14026704660008), received between Sep 29, 2026 and Sep 29, 2026.
The most frequently reported specific device problem is “Fluid/Blood Leak” (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.
Reports received per month
Most reported problems
Device problems
- Fluid/Blood Leak1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
OtherSep 29, 2026Fluid/Blood Leak
It was reported that during use in the neonatal intensive care unit, a large amount of fluid accumulated inside the HUDSON RCI brand heated breathing circuit set.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50933217 ↗
Other SET, TUBING AND SUPPORT, VENTILATOR (W HARNESS) devices
- Breathing circuit set, coaxial 260128Hamilton Medical AG · Set, Tubing And Support, Ventilator (W Harness)2 recalls10 reports
- Percussionaire P5-TEEPercussionaire Corporation · Set, Tubing And Support, Ventilator (W Harness)2 recalls1 report
- F&P FlexiTrunk BC191-05Fisher & Paykel Healthcare Limited · Set, Tubing And Support, Ventilator (W Harness)76 reports
- HUDSON RCI IPN043837Teleflex Incorporated · SET, TUBING AND SUPPORT, VENTILATOR (W HARNESS)1 recall18 reports
- Breathing circuit set, coaxial 260127Hamilton Medical AG · Set, Tubing And Support, Ventilator (W Harness)1 recall7 reports
- Breathing circuit set, coaxial 260168Hamilton Medical AG · Set, Tubing And Support, Ventilator (W Harness)1 recall4 reports
- Breathing circuit set, coaxial 260167Hamilton Medical AG · Set, Tubing And Support, Ventilator (W Harness)1 recall3 reports
- Vivo Series 006093Breas Medical AB · Set, Tubing And Support, Ventilator (W Harness)1 recall0 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.
How reports and recalls are matched · Editorial policy · Report an error on this page