HUDSON RCI IPN913687Recalls & reported problems
Teleflex Incorporated · Ventilator Tubing Set · Class 1
All models of HUDSON RCI (152)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 9
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 9 adverse event reports that list this exact device (DI 14026704658920), received between Apr 5, 2021 and Dec 2, 2021 — classified as 9 malfunctions.
The most frequently reported specific device problem is “Connection Problem” (5 reports).
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
- Connection Problem5
- Gas/Air Leak3
- Loose or Intermittent Connection1
Patient problems
- No Clinical Signs, Symptoms or Conditions9
Recent adverse event reports
The 9 most recent of 9 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 2, 2021Connection Problem; Connection Problem
IT WAS REPORTED "I HAVE HAD A FEW COMPLAINTS OVER THE LAST COUPLE OF WEEKS REGARDING OUR VENTILATOR CIRCUITS (REF: 1613).THE CONNECTOR PLUGS BECOME DISCONNECTED FROM THE TEMPERATURE PROBE PORTS". NO PATIENT INJURY OR HARM REPORTED. PATIENT CONDITION REPORTED AS "FINE".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12921266 ↗MalfunctionDec 2, 2021Connection Problem; Connection Problem
IT WAS REPORTED "I HAVE HAD A FEW COMPLAINTS OVER THE LAST COUPLE OF WEEKS REGARDING OUR VENTILATOR CIRCUITS (REF: 1613).THE CONNECTOR PLUGS BECOME DISCONNECTED FROM THE TEMPERATURE PROBE PORTS". NO PATIENT INJURY OR HARM REPORTED. PATIENT CONDITION REPORTED AS "FINE".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12921164 ↗MalfunctionDec 2, 2021Connection Problem; Connection Problem
IT WAS REPORTED "I HAVE HAD A FEW COMPLAINTS OVER THE LAST COUPLE OF WEEKS REGARDING OUR VENTILATOR CIRCUITS (REF: 1613).THE CONNECTOR PLUGS BECOME DISCONNECTED FROM THE TEMPERATURE PROBE PORTS". NO PATIENT INJURY OR HARM REPORTED. PATIENT CONDITION REPORTED AS "FINE".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12921104 ↗MalfunctionDec 2, 2021Connection Problem; Connection Problem
IT WAS REPORTED "I HAVE HAD A FEW COMPLAINTS OVER THE LAST COUPLE OF WEEKS REGARDING OUR VENTILATOR CIRCUITS (REF: 1613).THE CONNECTOR PLUGS BECOME DISCONNECTED FROM THE TEMPERATURE PROBE PORTS". NO PATIENT INJURY OR HARM REPORTED. PATIENT CONDITION REPORTED AS "FINE".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12921099 ↗MalfunctionDec 2, 2021Connection Problem; Connection Problem
IT WAS REPORTED "I HAVE HAD A FEW COMPLAINTS OVER THE LAST COUPLE OF WEEKS REGARDING OUR VENTILATOR CIRCUITS (REF: 1613).THE CONNECTOR PLUGS BECOME DISCONNECTED FROM THE TEMPERATURE PROBE PORTS". NO PATIENT INJURY OR HARM REPORTED. PATIENT CONDITION REPORTED AS "FINE".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12921025 ↗MalfunctionJul 20, 2021Gas/Air Leak; Gas/Air Leak
IT WAS REPORTED "THERE APPEARS TO BE A LEAK IN THE CIRCUIT. PATIENT WAS LOSING VOLUME FROM VENTILATOR. NO HOLE IS VISIBLE". NO PATIENT CONSEQUENCE OR INJURY REPORTED. PATIENT CONDITION REPORTED AS "FINE".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12196426 ↗MalfunctionMay 3, 2021Loose or Intermittent Connection; Loose or Intermittent Connection
IT WAS REPORTED "CUSTOMER STATES THE CUFF ADAPTOR ON THE EXPIRATORY LIMB APPEARS TO BE A LOOSE CONNECTION TO THEIR VENTILATOR EXPIRATION PORT". NO PATIENT INVOLVEMENT REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11761071 ↗MalfunctionApr 5, 2021Gas/Air Leak; Gas/Air Leak
IT WAS REPORTED "THE 1613 CIRCUIT COULDN'T PASS PRE USE CHECK ON THE PHILLIPS V200 VENTILATOR. HE SAYS IT LEAKED". NO PATIENT INVOLVEMENT REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11613455 ↗MalfunctionApr 5, 2021Gas/Air Leak; Gas/Air Leak
IT WAS REPORTED "THE 1613 CIRCUIT COULDN'T PASS PRE USE CHECK ON THE PHILLIPS V200 VENTILATOR. HE SAYS IT LEAKED". NO PATIENT INVOLVEMENT REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11613452 ↗
Other Circuit, breathing (w connector, adaptor, y piece) devices
- Medline Industries, Inc. DYNJ905503FMedline Industries, Inc. · Circuit, breathing (w connector, adaptor, y piece)3 recalls0 reports
- Medline Industries, Inc. PHS972096014BMedline Industries, Inc. · Circuit, breathing (w connector, adaptor, y piece)3 recalls0 reports
- Medline Industries, Inc. DYNJ0185290GMedline Industries, Inc. · Circuit, breathing (w connector, adaptor, y piece)3 recalls0 reports
- Medline Industries, Inc. DYNJ905503GMedline Industries, Inc. · Circuit, breathing (w connector, adaptor, y piece)2 recalls0 reports
- Medline Industries, Inc. DYNJAA262AMedline Industries, Inc. · Circuit, breathing (w connector, adaptor, y piece)2 recalls0 reports
- Medline Industries, Inc. DYNJ905567AMedline Industries, Inc. · Circuit, breathing (w connector, adaptor, y piece)2 recalls0 reports
- MEDLINE INDUSTRIES, INC. DYNJ86657AMedline Industries, Inc. · Circuit, breathing (w connector, adaptor, y piece)2 recalls0 reports
- Medline Industries, Inc. DYKMBNDL199AMedline Industries, Inc. · Circuit, breathing (w connector, adaptor, y piece)2 recalls0 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