AirLife 2K7000Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10885403220456), received between May 6, 2020 and May 6, 2020 — classified as 1 injury.

The most frequently reported specific device problem is “Defective Device” (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 16, 2026.

Most reported problems

Recent adverse event reports

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

• InjuryMay 6, 2020Defective Device; Defective Device

  THE CUSTOMER REPORTED THAT AFTER SUCCESSFULLY INTUBATING THE PATIENT IN THE CARDIO-THORACIC ICU, THE TEAM WAS UNABLE TO SEPARATE THE MASK FROM THE RESUSCITATION BAG OF AIRLIFE ADULT MANUAL RESUSCITATOR TO VENTILATE VIA THE ENDOTRACHEAL TUBE. THE TEAM WAS ABLE TO RESUME VENTILATION AND OXYGENATION WITH A NEW RESUSCITATION BAG. AT THIS TIME, PATIENT OUTCOME IS UNKNOWN.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 10029512 ↗