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Argyle 8888501007Recalls & reported problems

Cardinal Health, Inc. · Flexible Yankauer,Regular Capacity, No Vent · Class 2

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

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10884527019823), received between Nov 18, 2022 and Nov 18, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Decrease in Suction” (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

  • Decrease in Suction1

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.

  • MalfunctionNov 18, 2022Decrease in Suction; Decrease in Suction

    THE CUSTOMER REPORTED DURING THE ASPIRATIONS OF LIQUIDS IN THE ABDOMEN, THE CANNULA WAS BLOCKED SEVERAL TIMES WITH SOLID PARTICLE MATERIALS AND DID NOT ASPIRATE ADEQUATELY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 15825101 ↗

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.