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GreenLight™ 4603EURecalls & reported problems

Airlife · GreenLight™ Single Patient Use ISO Green Standard Stainless Steel Laryngoscope Blade · Class 1

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10190752147584), received between Nov 2, 2022 and Nov 2, 2022 — classified as 1 injury.

The most frequently reported specific device problem is “Disconnection” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Disconnection1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjuryNov 2, 2022Disconnection; Disconnection

    THE CUSTOMER REPORTED TO VYAIRE MEDICAL THAT BEFORE AND DURING ATTEMPTS TO INTUBATE THE PATIENT, THE BLADE, LARYN, STEEL, GREEN STD, MAC 3 WOULD SLIDE OUT AND SNAP OFF THE HANDLE WHEN IT WAS RAISED TO CLICK INTO THE HANDLE AND TURN ON THE LIGHT. THE CUSTOMER CONFIRMED NO HARM WAS DONE TO THE PATIENT ALTHOUGH IT REQUIRED TWO HANDS TO HOLD THE PRODUCT TOGETHER WHEN SWITCHING FROM STANDBY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 15718905 ↗

Other LARYNGOSCOPE, RIGID devices

All LARYNGOSCOPE, RIGID devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.