Argyle 8888160408Recalls & reported problems
Cardinal Health, Inc. · Umbilical Vessel Catheter Tray,No Catheter · Class 2
- Adverse event reports
- 8
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 8 adverse event reports that list this exact device (DI 10884527005147), received between Aug 11, 2020 and Aug 11, 2020 — classified as 8 malfunctions.
The most frequently reported specific device problem is “Crack” (8 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.
Most reported problems
Device problems
- Crack8
Patient problems
- No Consequences Or Impact To Patient8
Recent adverse event reports
The 8 most recent of 8 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 11, 2020Crack; Crack
THE CUSTOMER REPORTED THE STOPCOCKS ON THE UMBILICAL LINES ARE CRACKING. THERE WAS NO HARM TO THE PATIENT.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 10390884 ↗MalfunctionAug 11, 2020Crack; Crack
THE CUSTOMER REPORTED THE STOPCOCKS ON THE UMBILICAL LINES ARE CRACKING. THERE WAS NO HARM TO THE PATIENT.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 10390829 ↗MalfunctionAug 11, 2020Crack; Crack
THE CUSTOMER REPORTED THE STOPCOCKS ON THE UMBILICAL LINES ARE CRACKING. THERE WAS NO HARM TO THE PATIENT.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 10390760 ↗MalfunctionAug 11, 2020Crack; Crack
THE CUSTOMER REPORTED THE STOPCOCKS ON THE UMBILICAL LINES ARE CRACKING. THERE WAS NO HARM TO THE PATIENT.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 10390674 ↗MalfunctionAug 11, 2020Crack; Crack
THE CUSTOMER REPORTED THE STOPCOCKS ON THE UMBILICAL LINES ARE CRACKING. THERE WAS NO HARM TO THE PATIENT.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 10390536 ↗MalfunctionAug 11, 2020Crack; Crack
THE CUSTOMER REPORTED THE STOPCOCKS ON THE UMBILICAL LINES ARE CRACKING. THERE WAS NO HARM TO THE PATIENT.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 10390369 ↗MalfunctionAug 11, 2020Crack; Crack
THE CUSTOMER REPORTED THE STOPCOCKS ON THE UMBILICAL LINES ARE CRACKING. THERE WAS NO HARM TO THE PATIENT.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 10390322 ↗MalfunctionAug 11, 2020Crack; Crack
THE CUSTOMER REPORTED THE STOPCOCKS ON THE UMBILICAL LINES ARE CRACKING. THERE WAS NO HARM TO THE PATIENT.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 10390247 ↗
Other CATHETER, UMBILICAL ARTERY devices
- Argyle 8888160333Cardinal Health, Inc. · CATHETER, UMBILICAL ARTERY2 deaths66 reports
- Argyle 8888160333Cardinal Health 200, LLC · CATHETER, UMBILICAL ARTERY1 recall7 reports
- Argyle 8888160556Cardinal Health 200, LLC · CATHETER, UMBILICAL ARTERY1 recall1 report
- Argyle 8888160341Cardinal Health 200, LLC · CATHETER, UMBILICAL ARTERY1 recall1 report
- Argyle 8888160119Cardinal Health 200, LLC · CATHETER, UMBILICAL ARTERY1 recall0 reports
- Argyle 8888160648Cardinal Health 200, LLC · CATHETER, UMBILICAL ARTERY1 recall0 reports
- Argyle 8888160325Cardinal Health 200, LLC · CATHETER, UMBILICAL ARTERY1 recall0 reports
- Argyle 8888160341Cardinal Health, Inc. · CATHETER, UMBILICAL ARTERY36 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.