Aspiration Catheter 92796Recalls & reported problems
Avanos Medical, Inc. · Aspiration Catheter · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- 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 00350770927961), received between Oct 4, 2022 and Oct 4, 2022 — classified as 1 malfunction.
The most frequently reported specific device problem is “Difficult to Open or Close” (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.
Most reported problems
Device problems
- Difficult to Open or Close1
Patient problems
- Insufficient Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 4, 2022Difficult to Open or Close
WE WENT TO USE THE ASPIRATION CATHETER DURING AN EGD THIS MORNING AND THE TIP WOULD NOT OPEN AND CLOSE IN ORDER TO GET THE ASPIRATE WE NEEDED FROM THE DUODENUM. WE HAD TO WASTE THIS SUPPLY AND OPEN A NEW ONE. FDA SAFETY REPORT ID# (B)(4).
Patient problems: Insufficient Information
MAUDE report 15543039 ↗
Other CATHETER (GASTRIC, COLONIC, ETC.), IRRIGATION AND ASPIRATION devices
- Argyle 8888750018Cardinal Health, Inc. · CATHETER (GASTRIC, COLONIC, ETC.), IRRIGATION AND ASPIRATION3 reports
- Argyle 8886864604Cardinal Health, Inc. · CATHETER (GASTRIC, COLONIC, ETC.), IRRIGATION AND ASPIRATION2 reports
- Halyard 92774Avanos Medical, Inc. · CATHETER (GASTRIC, COLONIC, ETC.), IRRIGATION AND ASPIRATION1 report
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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