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Argyle 8888505024Recalls & reported problems

Cardinal Health 200, LLC · Argyle Yankauer Bulb Tip with Vent · Class 2

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 10884527019953), received between Aug 18, 2021 and Aug 18, 2021 — classified as 1 injury.

The most frequently reported specific device problem is “Component Missing” (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

  • Component Missing1

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.

  • InjuryAug 18, 2021Component Missing; Component Missing

    THE CUSTOMER REPORTED THE YANKAEUR SUCTION BULB TIP SHEARED OFF OR WAS MISSING. THEY ARE UNSURE WHETHER THIS WAS BEFORE USE. ADDITIONAL INFORMATION RECEIVED STATED THERE WAS ONLY ONE YANKAEUR AFFECTED. THE STAFF MEMBERS CONCERNED DO NOT THINK THAT ANY OF THE TIP WAS LEFT IN THE PATIENT. THE PATIENT DID HOWEVER RECEIVE A VIDEO BRONCHOSCOPE AND CMAC LARYNGOSCOPY WHILE STILL ANAESTHETIZED AND INTUBATED TO INSPECT AND CONFIRM ANY EVIDENCE OF ANY PLASTIC REMAINING. NO EVIDENCE OF A FOREIGN BODY WAS FOUND. THERE WAS NO HARM TO THE PATIENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 12338949 ↗

Other APPARATUS, SUCTION, OPERATING-ROOM, WALL VACUUM POWERED devices

All APPARATUS, SUCTION, OPERATING-ROOM, WALL VACUUM POWERED devices →

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