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SHERIDAN IPN926927Recalls & reported problems

Teleflex Incorporated · ET TUBE,CF,8.0 · Class 2

All models of SHERIDAN (19)

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 14026704759153), received between Mar 24, 2023 and Jul 25, 2023 — classified as 3 malfunctions.

The most frequently reported specific device problem is “Break” (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

  • Break1
  • Inflation Problem1
  • Leak/Splash1

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.

  • MalfunctionJul 25, 2023Inflation Problem; Inflation Problem

    IT WAS REPORTED THAT "THE CUFF DIDN'T INFLATE WHEN INTUBATING THE TUBE TO THE PATIENT. THEREFORE, THE TUBE WAS REPLACED WITH A NEW ONE. NO INJURY TO THE PATIENT WAS REPORTED." NO PATIENT HARM OR INJURY. THE PATIENT STATUS IS REPORTED AS "FINE".

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 17389306 ↗
  • MalfunctionJun 8, 2023Break; Break

    IT WAS REPORTED THAT "THE DOCTOR FOUND CONNECTOR BROKEN WHEN USING ON PATIENT. THEN CHANGED NEW ONE, NO IMPACT ON PATIENT". NO PATIENT HARM OR INJURY. THE PATIENT STATUS IS REPORTED AS "FINE".

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 17089859 ↗
  • MalfunctionMar 24, 2023Leak/Splash; Leak/Splash

    REPORTED ISSUE: WHILE INTUBATING PATIENT THE CUFF WOULD NOT STAY INFLATED. IT DID NOT CAUSE ANY ISSUES. THEY REMOVED THE TUBE AND PLACED A SIZE 7.5 TUBE WITH NO ISSUES.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 16615843 ↗

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-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-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-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-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-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-1956-2019 · Jun 7, 2019 · Terminated
    Sheridan Endotracheal Tube contained inside Centurion kit code TC7855.
  • Z-1759-2019 · May 24, 2019 · Terminated
    Hudson RCI Sheridan LTS, Product Code 5-11112 Product Usage: Tracheal tube/airway management
  • 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-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-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-1760-2019 · May 24, 2019 · Terminated
    Hudson RCI Sheridan: 1) CF 6.0 mm, Product Codes: 5-10112, 5-10212 2) CF 6.5 mm, Product Codes: 5-10113, 5-10213 3) CF 7.0 mm, Product Codes: 5-10114, 5-10214 4) CF 7.5 mm,
  • Z-1764-2019 · May 24, 2019 · Terminated
    Hudson RCI Sheridan: 1) HVT 6.0 mm, Product Code 5-10312 2) HVT 6.5 mm, Product Code 5-10313 3) HVT 7.0 mm, Product Code 5-10314 4) HVT 7.5 mm, Product Code 5-10315 5) HVT 8.0

…and 12 more.

Other Tube, tracheal (w/wo connector) devices

All Tube, tracheal (w/wo connector) devices →

Sources and updates

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