Argyle 31000Recalls & reported problems
Cardinal Health 200, LLC · Arygle Suction Catheter with Chimney Valve Striaght Packed 10 Fr/ Ch · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10192253041989), received between Oct 16, 2025 and Mar 23, 2026 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Break” (2 reports).
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.
Reports received per month
Most reported problems
Device problems
- Break2
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 23, 2026Break
THE CUSTOMER REPORTED THE SUCTION CATHETER TOP SNAPPED OFF WHEN PATIENT WAS HAVING DESATS. THERE WAS NO PATIENT HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24662504 ↗MalfunctionOct 16, 2025Break; Break
CUSTOMER REPORTS: WHEN ATTEMPTING TO USE SUCTION DURING RESUSCITATION AFTER DELIVERY OF A BABY, THE SUCTION CATHETER WAS FOUND BROKEN WHERE THE CATHETER MEETS THE PLASTIC THUMB PORT PORTION. ACCORDING TO THE REPORT, THERE WAS NO SERIOUS HARM REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23310103 ↗
Other CATHETER AND TIP, SUCTION devices
- J-VAC 2160Ethicon Inc. · CATHETER AND TIP, SUCTION152 reports
- Wayne G56537Cook Incorporated · CATHETER AND TIP, SUCTION2 recalls33 reports
- Bard® Suction Connector EN0066000C. R. Bard, Inc. · CATHETER AND TIP, SUCTION1 recall6 reports
- Argyle 10142Cardinal Health 200, LLC · CATHETER AND TIP, SUCTION1 recall0 reports
- Argyle 12191Cardinal Health 200, LLC · CATHETER AND TIP, SUCTION1 recall0 reports
- Medline Industries, Inc. OR929KMedline Industries, Inc. · CATHETER AND TIP, SUCTION1 recall0 reports
- Argyle 12102Cardinal Health 200, LLC · CATHETER AND TIP, SUCTION1 recall0 reports
- Argyle 10102Cardinal Health 200, LLC · CATHETER AND TIP, SUCTION1 recall0 reports
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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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