Medline DYNSCS20100Recalls & reported problems
Medline Industries, Inc. · CATHETER,IV,SURESITE SLIDE,20G X 1" · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10888277667525), received between Sep 21, 2021 and Sep 29, 2026 — classified as 1 injury, 2 malfunctions.
The most frequently reported specific device problem is “Break” (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.
Reports received per month
Most reported problems
Device problems
- Break1
- Dull, Blunt1
- Entrapment of Device1
- Material Integrity Problem1
- Protective Measures Problem1
Patient problems
- Foreign Body In Patient1
- Hemorrhage/Blood Loss/Bleeding1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 29, 2026Dull, Blunt; Protective Measures Problem
It was reported that "they are not sharp enough, and the safety feature does not always work."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50934521 ↗MalfunctionSep 29, 2023Material Integrity Problem; Material Integrity Problem
InjurySep 21, 2021Break; Entrapment of Device
IT WAS REPORTED THAT THE CATHETER BROKE OFF INSIDE OF THE PATIENTS HAND AFTER INSERTION.
Patient problems: Foreign Body In Patient
MAUDE report 12506012 ↗
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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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