LMA AIRWAY MANAGEMENTRecalls & reported problems across all models

We found 47 models of LMA AIRWAY MANAGEMENT by Teleflex Incorporated in the FDA's device registry (GUDID). Together they are named in 139 adverse event reports in the FDA's MAUDE database, received between Oct 24, 2017 and May 21, 2026 — classified as 7 injuries, 132 malfunctions.

The most frequently reported specific device problem is “Gas/Air Leak” (45 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. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works

Most reported LMA AIRWAY MANAGEMENT problems

LMA AIRWAY MANAGEMENT models

47 models, most reported first. Each model has its own page with its reports, recalls and device details.

• LMA AIRWAY MANAGEMENT IPN922810

  AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY
  21 reports
• LMA AIRWAY MANAGEMENT IPN902073

  AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY
  15 reports
• LMA AIRWAY MANAGEMENT IPN922811

  AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY
  12 reports
• LMA AIRWAY MANAGEMENT IPN902070

  AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY
  8 reports
• LMA AIRWAY MANAGEMENT IPN922772

  AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY
  6 reports
• LMA AIRWAY MANAGEMENT IPN922818

  AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY
  5 reports
• LMA AIRWAY MANAGEMENT IPN917164

  AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY
  5 reports
• LMA AIRWAY MANAGEMENT IPN041107

  AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY
  4 reports
• LMA AIRWAY MANAGEMENT IPN922773

  AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY
  4 reports
• LMA AIRWAY MANAGEMENT IPN922891

  AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY
  4 reports
• LMA AIRWAY MANAGEMENT IPN924140

  AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY
  4 reports
• LMA AIRWAY MANAGEMENT IPN902076

  AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY
  3 reports
• LMA AIRWAY MANAGEMENT IPN047898

  AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY
  3 reports
• LMA AIRWAY MANAGEMENT IPN047595

  AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY
  3 reports
• LMA AIRWAY MANAGEMENT IPN917163

  AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY
  3 reports
• LMA AIRWAY MANAGEMENT IPN039839

  AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY
  2 reports
• LMA AIRWAY MANAGEMENT IPN922790

  AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY
  2 reports
• LMA AIRWAY MANAGEMENT IPN922900

  AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY
  2 reports
• LMA AIRWAY MANAGEMENT IPN923208

  AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY
  2 reports
• LMA AIRWAY MANAGEMENT IPN924137

  AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY
  2 reports
• LMA AIRWAY MANAGEMENT IPN924139

  AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY
  2 reports
• LMA AIRWAY MANAGEMENT IPN924052

  AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY
  2 reports
• LMA AIRWAY MANAGEMENT IPN901799

  AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY
  1 report
• LMA AIRWAY MANAGEMENT IPN901828

  AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY
  1 report
• LMA AIRWAY MANAGEMENT IPN902063

  AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY
  1 report
• LMA AIRWAY MANAGEMENT IPN914129

  AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY
  1 report
• LMA AIRWAY MANAGEMENT 105300-000050

  AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY
  1 report
• LMA AIRWAY MANAGEMENT IPN056623

  AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY
  1 report
• LMA AIRWAY MANAGEMENT IPN922798

  AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY
  1 report
• LMA AIRWAY MANAGEMENT IPN922058

  AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY
  1 report
• LMA AIRWAY MANAGEMENT IPN922781

  AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY
  1 report
• LMA AIRWAY MANAGEMENT IPN922816

  AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY
  1 report
• LMA AIRWAY MANAGEMENT IPN922801

  AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY
  1 report
• LMA AIRWAY MANAGEMENT IPN922807

  AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY
  1 report
• LMA AIRWAY MANAGEMENT IPN922808

  AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY
  1 report
• LMA AIRWAY MANAGEMENT IPN922800

  AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY
  1 report
• LMA AIRWAY MANAGEMENT IPN922769

  AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY
  1 report
• LMA AIRWAY MANAGEMENT IPN916566

  AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY
  1 report
• LMA AIRWAY MANAGEMENT IPN922892

  AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY
  1 report
• LMA AIRWAY MANAGEMENT IPN923207

  AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY
  1 report
• LMA AIRWAY MANAGEMENT IPN923209

  AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY
  1 report
• LMA AIRWAY MANAGEMENT IPN923211

  AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY
  1 report
• LMA AIRWAY MANAGEMENT IPN923480

  AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY
  1 report
• LMA AIRWAY MANAGEMENT IPN924141

  AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY
  1 report
• LMA AIRWAY MANAGEMENT IPN924147

  AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY
  1 report
• LMA AIRWAY MANAGEMENT IPN924148

  AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY
  1 report
• LMA AIRWAY MANAGEMENT IPN917162

  AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY
  1 report

Recent LMA AIRWAY MANAGEMENT adverse event reports

The 15 most recent reports across all models, in the reporter's own words as published by the FDA.

• MalfunctionMay 21, 2026Deflation Problem; Inflation Problem

  IT WAS REPORTED THAT "THE LMA CUFF WAS NOT INFLATING OR DEFLATING." NO PATIENT INVOLVEMENT. TWO UNITS REPORTED. ASSOCIATED MDRS: 3009307931-2026-00018.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25246450 ↗
• MalfunctionMay 21, 2026Deflation Problem; Inflation Problem

  IT WAS REPORTED THAT "THE LMA CUFF WAS NOT INFLATING OR DEFLATING." NO PATIENT INVOLVEMENT. TWO UNITS REPORTED. ASSOCIATED MDRS: 3009307931-2026-00019.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25246442 ↗
• MalfunctionMay 6, 2026Product Quality Problem

  IT WAS REPORTED THAT "MASK WITH UNSATISFACTORY SEALING PERFORMANCE." NO PATIENT INVOLVEMENT. NO ADDITIONAL INFORMATION AVAILABLE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25099262 ↗
• MalfunctionApr 14, 2026Inflation Problem

  IT WAS REPORTED THAT: "(B)(6) 2026, THE DOCTOR FOUND CUFF CANNOT INFLATE WHEN DOING TESTING BEFORE USING ON PATIENT. CHANGE NEW TUBE."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24873107 ↗
• MalfunctionApr 2, 2026Leak/Splash

  IT WAS REPORTED THAT"(B)(6) 2026, THE DOCTOR FOUND CUFF LEAKAGE WHEN DOING TESTING BEFORE USING ON PATIENT. CHANGE NEW TUBE."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24765275 ↗
• MalfunctionMar 30, 2026Inflation Problem

  IT WAS REPORTED THAT: "LMA WAS USED IN THE INTUBATION OF A PATIENT, BUT IT WOULDN'T STAY INFLATED. A NEW ONE WAS OBTAINED AND WORKED. NO PATIENT HARM REPORTED.".

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24727618 ↗
• MalfunctionMar 23, 2026Gas/Air Leak

  IT WAS REPORTED THAT"(B)(6) 2026, THE DOCTOR FOUND CUFF LEAKAGE WHEN USING ON PATIENT. TUBE REMOVED AND CHANGED TO A NEW ONE. PATIENT IS REPORTED AS FINE."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24660637 ↗
• MalfunctionFeb 12, 2026Material Separation

  IT WAS REPORTED THAT "THE LMA CAME APART. THE CUFF OF THE LMA EVO SEPARATED FROM THE DEVICE AND WAS IN THE PATIENT'S AIRWAY (THEY HAD TO PULL IT OUT). NO DAMAGE DONE TO THE PATIENT."

  Patient problems: Foreign Body In Patient

  MAUDE report 24321281 ↗
• MalfunctionFeb 12, 2026Leak/Splash

  IT WAS REPORTED THAT: "(B)(6) 2026, THE DOCTOR FOUND CUFF LEAKAGE WHEN DOING TESTING BEFORE USING ON PATIENT. CHANGE NEW TUBE."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24320528 ↗
• MalfunctionJan 26, 2026Inflation Problem

  IT WAS REPORTED THAT: "PRIOR TO USE, INSPECTION. FOUND COULD NOT INFLATE CUFF".

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24176085 ↗
• MalfunctionJan 16, 2026Gas/Air Leak

  IT WAS REPORTED THAT: "(B)(6) 2025, THE DOCTOR FOUND CUFF LEAKAGE WHEN USING ON PATIENT. CHANGE NEW TUBE. THE PATIENT WAS REPORTED AS FINE. THERE WAS NO REPORTED HARM OR CONSEQUENCE.".

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24092906 ↗
• MalfunctionJan 16, 2026Fluid/Blood Leak

  IT WAS REPORTED THAT: "(B)(6) 2025, THE DOCTOR FOUND CUFF LEAKAGE WHEN DOING TESTING BEFORE USING ON PATIENT. CHANGE NEW TUBE. IT DID NOT AFFECT THE PROGRESS OF THE SURGERY."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24092076 ↗
• MalfunctionJan 9, 2026Gas/Air Leak; Unintended Deflation

  IT WAS REPORTED THAT: "(B)(6) 2025, THE DOCTOR FOUND CUFF LEAKAGE WHEN DOING TESTING BEFORE USING ON PATIENT. AFTER INFLATING THE SYRINGE, THE BALLOON CANNOT MAINTAIN PRESSURE. CHANGE NEW TUBE."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24018500 ↗
• MalfunctionJan 2, 2026Material Separation

  IT WAS REPORTED THAT: "A FAULTY SUPREME LMA THAT WAS USED IN SURGERY AT MD ANDERSON CANCER CENTER, CAME APART, CAUSING A SIGNIFICANT LEAK DURING A PROCEDURE".

  Patient problems: Insufficient Information

  MAUDE report 23943748 ↗
• InjuryDec 31, 2025Patient Device Interaction Problem; Patient Device Interaction Problem

  IT WAS REPORTED THAT: "PATIENT WAS EMERGING FROM ANESTHESIA POST RIGHT RING FINGER ORIF. DURING EXTUBATION THE PATIENT BIT DOWN AT THE POINT OF CONNECTION BETWEEN THE MASK AND THE SHAFT OF THE TUBE. THE MASK BECAME LODGED IN THE PATIENT'S AIRWAY CAUSING FLASH PULMONARY EDEMA WHICH REQUIRED TRANSPORT AND ADMISSION TO A LOCAL HOSPITAL FOR STABILIZATION, PATIENT WAS DISCHARGED 2 DAYS LATER".

  Patient problems: Pulmonary Edema

  MAUDE report 23932471 ↗

Other Teleflex Incorporated products

• ARROW1,494 models · 9,043 reports · 62 recalls
• RUSCH220 models · 436 reports · 130 recalls
• WECK97 models · 3,790 reports · 1 recall
• HUDSON RCI152 models · 1,461 reports · 7 recalls
• LANGSTON4 models · 15 reports · 5 recalls
• PLEUR-EVAC15 models · 146 reports · 1 recall
• UROLIFT13 models · 137 reports
• GIBECK7 models · 32 reports · 2 recalls