Argyle 8888301713Recalls & reported problems
Cardinal Health, Inc. · Argyle Suction Tubing Molded Connectors 9/32" x 10' (7 mm x 3.1 m) · Class 2
All models of Argyle (64)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 11
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 11 adverse event reports that list this exact device (DI 10884527019700), received between Nov 11, 2019 and Feb 25, 2025 — classified as 11 malfunctions.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (10 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 Component10
- Suction Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions9
- No Consequences Or Impact To Patient1
- No Patient Involvement1
Recent adverse event reports
The 11 most recent of 11 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 25, 2025Detachment of Device or Device Component; Detachment of Device or Device Component
THE CUSTOMER REPORTED THAT THE CONNECTORS WERE DISENGAGED. THE PRODUCT WAS UNUSED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21465441 ↗MalfunctionOct 23, 2024Detachment of Device or Device Component; Detachment of Device or Device Component
THE CUSTOMER REPORTED THAT THE JOINT CONNECTORS WERE DISENGAGED. THE PRODUCT WAS UNUSED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20518143 ↗MalfunctionOct 23, 2024Detachment of Device or Device Component; Detachment of Device or Device Component
THE CUSTOMER REPORTED THAT THE JOINT CONNECTORS ARE DISLOCATED. THE PRODUCT WAS UNUSED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20517656 ↗MalfunctionOct 23, 2024Detachment of Device or Device Component; Detachment of Device or Device Component
THE CUSTOMER REPORTED THAT THE JOINT CONNECTORS WERE DISENGAGED. THE PRODUCT WAS UNUSED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20517564 ↗MalfunctionSep 22, 2023Suction Problem; Suction Problem
THE CUSTOMER REPORTED THAT DURING OPERATION, THE SUCTION DID NOT WORK. WHEN CONFIRMING, IT LOOKED LIKE A FILM WAS FORMED INSIDE THE CONNECTING PART ON ONE END; PERIOD OF USE WAS A FEW MINUTES. THERE WAS NO PATIENT INJURY REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17799219 ↗MalfunctionJun 15, 2021Detachment of Device or Device Component; Detachment of Device or Device Component
THE CUSTOMER REPORTED THE BLUE CONNECTOR HAS NOT BEEN GLUED, IT WAS DETACHED IN THE UNOPENED PACKAGE. THE DEVICE WAS NOT USED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12000625 ↗MalfunctionMar 2, 2021Detachment of Device or Device Component; Detachment of Device or Device Component
THE CUSTOMER REPORTED THAT THE BLUE SUREGRIP WAS FOUND TO BE DETACHED FROM THE TUBING WHEN THE PRODUCT WAS TAKEN OUT OF THE INDIVIDUAL PACKAGE, THERE APPEARED TO BE A BONDING FAILURE. THERE WAS NO PATIENT INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11400055 ↗MalfunctionJan 11, 2021Detachment of Device or Device Component; Detachment of Device or Device Component
THE CUSTOMER REPORTED THAT THE SURE GRIP (BLUE CONNECTOR) ON THE TIP OF TUBING CAME OFF AT THE START OF USE. THERE WAS NO PATIENT HARM REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11147759 ↗MalfunctionDec 22, 2020Detachment of Device or Device Component; Detachment of Device or Device Component
THE CUSTOMER REPORTED THE BLUE SUREGRIP CONNECTOR WAS DETACHED WHEN THE PACKAGE WAS OPENED. THERE WAS NO PATIENT INVOLVED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11056846 ↗MalfunctionOct 19, 2020Detachment of Device or Device Component; Detachment of Device or Device Component
THE CUSTOMER STATES THAT THE BLUE CONNECTOR WAS NOT BONDED AND IT CAME OFF.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 10698250 ↗MalfunctionNov 11, 2019Detachment of Device or Device Component; Detachment of Device or Device Component
THE CUSTOMER REPORTED THAT THE BLUE CONNECTOR CAME OFF WHEN THEY TRIED TO USE IT. IT WAS NOTICED BEFORE USE. NO PATIENT INVOLVED.
Patient problems: No Patient Involvement
MAUDE report 9304402 ↗
Other TUBING, NONINVASIVE devices
- Argyle 8888301614Cardinal Health, Inc. · TUBING, NONINVASIVE14 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
- Argyle 8888301606Cardinal Health, 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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