Argyle 8888301606Recalls & reported problems
Cardinal Health, Inc. · Argyle Suction Tubing Integral Funnel/Funnel 1/4" x 6' (6 mm x 1.8 m) · Class 2
All models of Argyle (64)
Data updated Oct 16, 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 10884527019649), received between Sep 7, 2023 and Jan 2, 2024 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Device problems
- Detachment of Device or Device Component2
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.
MalfunctionJan 2, 2024Detachment of Device or Device Component; Detachment of Device or Device Component
THE CUSTOMER REPORTED THAT THE BLUE CONNECTOR DISENGAGED EASILY. IT DOES NOT APPEAR TO BE BARELY GLUED. PER ADDITIONAL INFORMATION RECEIVED, THERE WAS NO MEDICAL INTERVENTION REQUIRED. THE PRODUCT WAS UNUSED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18425783 ↗MalfunctionSep 7, 2023Detachment of Device or Device Component; Detachment of Device or Device Component
CUSTOMER REPORTS: THE SURE-GRIP COMES OFF. ABOUT 80% OF THE PRODUCT DISENGAGES FROM THE SURE-GRIP, THUS, THE CUSTOMER USES THE PRODUCT BY CUTTING OFF THE SURE-GRIP PART. THE PERIOD OF USE IS 1 TO 3 DAYS. THERE WAS NO PATIENT INJURY. PER ADDITIONAL INFORMATION PROVIDED ON (B)(6) 2023, THE SURE GRIP HAS BEEN IDENTIFIED AS THE BLUE CONNECTOR WHICH DID DETACH. IT APPEARS THAT THE CONNECTOR WAS LOOSE, MOST LIKELY DUE TO INSUFFICIENT ADHESIVE. THERE WAS NO MEDICAL INTERVENTION REQUIRED. THE NUMBER OF PATIENTS IS UNKNOWN.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17698337 ↗
Other TUBING, NONINVASIVE devices
- Argyle 8888301614Cardinal Health, Inc. · TUBING, NONINVASIVE14 reports
- Argyle 8888301713Cardinal Health, Inc. · TUBING, NONINVASIVE11 reports
- Argyle 5558301627Cardinal Health, Inc. · TUBING, NONINVASIVE3 reports
- MEDLINE DYND50252Medline Industries, Inc. · TUBING, NONINVASIVE3 reports
- Argyle 8888301523Cardinal Health, Inc. · TUBING, NONINVASIVE3 reports
- MEDLINE DYND50251Medline Industries, Inc. · TUBING, NONINVASIVE2 reports
- NA SVT-089Boston Scientific Corporation · TUBING, NONINVASIVE2 reports
- CARDINAL HEALTH N510Cardinal Health 200, LLC · TUBING, NONINVASIVE1 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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