LMA AIRWAY MANAGEMENT IPN924052Recalls & reported problems
Teleflex Incorporated · LMA® Flexible PreCurved™ Airway with Cuff Pilot™ Technology Size 4 · Class 1
All models of LMA AIRWAY MANAGEMENT (47)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 15060112319720), received between Dec 4, 2024 and Apr 24, 2025 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Deflation Problem” (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
- Deflation Problem1
- Gas/Air Leak1
- Inflation Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 24, 2025Deflation Problem; Gas/Air Leak; Deflation Problem; Gas/Air Leak
IT WAS REPORTED THAT: "WHEN THE USER ATTEMPTED TO USE THE DEVICE, THE CUFF DEFLATED. IT SEEMED THAT AIR WAS LEAKING FROM SOMEWHERE OF THE CUFF. THEREFORE, A NEW UNIT WAS USED INSTEAD. THE ISSUE OCCURRED BEFORE USE ON A PATIENT."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21898352 ↗MalfunctionDec 4, 2024Inflation Problem; Inflation Problem
IT WAS REPORTED THAT "THE USER ATTEMPTED TO INFLATE THE CUFF DURING USE, BUT AIR WOULD NOT COME INTO IT. THEREFORE, A NEW UNIT WAS USED INSTEAD. NO INJURY TO THE PATIENT OCCURRED".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20844554 ↗
Other AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY devices
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- Medline DYND300015PMedline Industries, Inc. · AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY1 recall0 reports
- KING LTS-D Kit KLTSD430King Systems Corporation · AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY1 recall0 reports
- Medline DYND300040PMedline Industries, Inc. · AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY1 recall0 reports
- King LTS-D KLTSD421King Systems Corporation · AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY1 recall0 reports
- ONE-PIECE GUEDEL AIRWAY, SIZE 3, ISO 9 1113090Intersurgical Incorporated · Airway, Oropharyngeal, Anesthesiology1 recall0 reports
- KING LTS-D Kit KLTSD432King Systems Corporation · AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY1 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.
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