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HUDSON RCI IPN048894Recalls & reported problems

Teleflex Incorporated · ET TUBE, HVT, 6.5 · Class 2

All models of HUDSON RCI (152)

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
3
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 14026704616739), received between Sep 17, 2021 and Apr 22, 2022 — classified as 3 malfunctions.

The most frequently reported specific device problem is “Deflation Problem” (1 report).

27 other recalls cover devices cleared under the same FDA submission (K822082); they may or may not involve this specific model.

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

  • Deflation Problem1
  • Gas/Air Leak1
  • Material Deformation1

Patient problems

  • No Clinical Signs, Symptoms or Conditions3

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

  • MalfunctionApr 22, 2022Deflation Problem; Deflation Problem

    IT WAS REPORTED THAT: "THE INCIDENT INVOLVED A FEMALE PATIENT. THE CUFF REMAINED INFLATED DURING REMOVAL, WHEREAS THE PILOT BALLOON WAS COMPLETELY DEFLATED WITH THE SYRINGE". NO PATIENT INJURY OR HARM REPORTED. PATIENT CONDITION REPORTED AS "FINE".

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 14190194 ↗
  • MalfunctionFeb 3, 2022Material Deformation; Material Deformation

    IT WAS REPORTED "[PILOT BALLOON] WAS DEFORMED SO [IT] COULD NOT [BE] USED". NO PATIENT INVOLVEMENT REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 13446622 ↗
  • MalfunctionSep 17, 2021Gas/Air Leak; Gas/Air Leak

    IT WAS REPORTED ""THE CUFF [WAS] FOUND LEAKING DURING THE INSPECTION". NO PATIENT INVOLVEMENT REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 12488013 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K822082. One submission often covers many models, so check the product and lot details in each record.

  • Z-2314-2019 · Jul 30, 2019 · Terminated
    Hudson RCI Sheridan Preformed: a) 3.0 mm, REF 5-22006, REF 5-22106 b) 3.5 mm, REF 5-22007, REF 5-22107 c) 4.0 mm, REF 5-22008, REF 5-22108, REF 5-22208 d) 4.5 mm, REF 5-22009,
  • Z-2316-2019 · Jul 30, 2019 · Terminated
    Hudson RCI Sheridan/HVT: a) 5.0 mm, REF 5-10310 b) 5.5 mm, REF 5-10311 c) 6.0 mm, REF 5-10312 d) 6.5 mm, REF 5-10313 e) 7.0 mm, REF 5-10314 f) 7.5 mm, REF 5-10315 g) 8.0 mm,
  • Z-2313-2019 · Jul 30, 2019 · Terminated
    Hudson RCI Sheridan EZ-ENDO: a) 5.0 mm, REF 5-22510 b) 5.5 mm, REF 5-22511 c) 7.0 mm, REF 5-22514 d) 7.5 mm, REF 5-22515 e) 8.0 mm, REF 5-22516 f) 8.5 mm, REF 5-22517 g) 9.0
  • Z-2315-2019 · Jul 30, 2019 · Terminated
    Hudson RCI Sheridan Uncuffed: a) 2.0 mm, REF 5-10404 b) 2.5 mm, REF 5-10405 c) 3.0 mm, REF 5-10406 d) 3.5 mm, REF 5-10407 e) 4.0 mm, REF 5-10408 f) 4.5 mm, REF 5-10409 g)
  • Z-2317-2019 · Jul 30, 2019 · Terminated
    Sheridan/CF Novaplus 7.0 mm, REF V5-10114 Product Usage: Tracheal tube/airway management
  • Z-2312-2019 · Jul 30, 2019 · Terminated
    Hudson RCI Sheridan/CF: a) 3.0 mm, REF 5-10106, REF 5-10206 b) 3.5 mm, REF 5-10107 c) 4.0 mm, REF 5-10108, REF 5-10208 d) 4.5 mm, REF 5-10109 e) 5.0 mm, REF 5-10110, REF 5-10
  • Z-2311-2019 · Jul 30, 2019 · Terminated
    Hudson RCI Sheridan LTS: a) 4.0 mm, REF 5-11108 b) 5.0 mm, REF 5-11110 c) 6.0 mm, REF 5-11112 Product Usage: Tracheal tube/airway management
  • Z-2318-2019 · Jul 30, 2019 · Terminated
    Sheridan/HVT Novaplus: a) 7.0 mm, REF V5-10314 b) 7.5 mm, REF V5-10315 c) 8.0 mm, REF V5-10316 d) 8.5 mm, REF V5-10317 Product Usage: Tracheal tube/airway management
  • Z-1956-2019 · Jun 7, 2019 · Terminated
    Sheridan Endotracheal Tube contained inside Centurion kit code TC7855.
  • Z-1761-2019 · May 24, 2019 · Terminated
    Hudson RCI Sheridan: 1) EZ-ENDO 6.0 mm, Product Code 5-22512 2) EZ-ENDO 6.5 mm, Product Code 5-22513 3) EZ-ENDO 7.0 mm, Product Code 5-22514 4) EZ-ENDO 7.5 mm, Product Code 5-2
  • Z-1763-2019 · May 24, 2019 · Terminated
    Hudson RCI Sheridan: 1) Uncuffed 6.0 mm, Product Code 5-10412 2) Uncuffed 6.5 mm, Product Code 5-10413 3) Uncuffed 7.0 mm, Product Code 5-10414 Product Usage: Tracheal tube/
  • Z-1762-2019 · May 24, 2019 · Terminated
    Hudson RCI Sheridan: 1) Preformed 6.0 mm, Product Codes: a) 5-22212, b) 5-22312, c) 5-22112, d) 5-22012, 2) Preformed 6.5 mm, Product Codes: a) 5-22313, b) 5-222
  • Z-1766-2019 · May 24, 2019 · Terminated
    Sheridan/HVT: 1) Novaplus 7.0 mm, Product Code V5-10314 2) Novaplus 7.5 mm, Product Code V5-10315 3) Novaplus 8.0 mm, Product Code V5-10316 4) Novaplus 8.5 mm, Product Code V5-
  • Z-1765-2019 · May 24, 2019 · Terminated
    Sheridan/CF Novaplus 7.0 mm, Product Code V5-10114 Product Usage: Tracheal tube/airway management
  • Z-1759-2019 · May 24, 2019 · Terminated
    Hudson RCI Sheridan LTS, Product Code 5-11112 Product Usage: Tracheal tube/airway management

…and 12 more.

Other Tube, tracheal (w/wo connector) devices

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Sources and updates

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