Halyard 92774Recalls & reported problems
Avanos Medical, Inc. · HALYARD* Injection Needle Catheter · Class 2
All models of Halyard (232)
Data updated Oct 16, 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 10680651927740), received between Jun 5, 2019 and Jun 5, 2019 — classified as 1 malfunction.
The most frequently reported specific device problem is “Failure to Deliver” (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
Device problems
- Failure to Deliver1
Patient problems
- No Code Available1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 5, 2019Failure to Deliver; Failure to Deliver
IT WAS REPORTED THAT "EGD [ESOPHAGOGASTRODUODENOSCOPY] IN EPI [EPINEPHRINE] NEEDLE WILL NOT DEPLOY."
Patient problems: No Code Available
MAUDE report 8670947 ↗
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
- Aspiration Catheter 92796Avanos 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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