Medline DYNSCA20100Recalls & reported problems
Medline Industries, Inc. · CATHETER, IV, SURESITE AUTO, 20G X 1.00" · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10888277667440), received between Feb 16, 2022 and Nov 24, 2023 — classified as 2 injuries.
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
Patient problems
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available1
- Foreign Body In Patient1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryNov 24, 2023Break; Break
ACCORDING TO THE CUSTOMER, ON (B)(6) 2023 AFTER INSERTING AN INTRAVENOUS CATHETER THE NURSE NOTED THE "HUB HAD BLOOD LEAKAGE AND MOVED TOO FREELY UNDER THE TEGADERM". THE CUSTOMER REPORTED AFTER REMOVING THE TEGADERM SHE NOTED THE CATHETER WAS NOT CONNECTED TO THE HUB.
Patient problems: Foreign Body In Patient
MAUDE report 18207533 ↗InjuryFeb 16, 2022Dull, Blunt
IT WAS REPORTED BY THE CUSTOMER THAT THE INTRAVENOUS CATHETERS ARE DULL AND THE NURSES ARE "HAVING TO RE-STICK THE PATIENT."
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 13545866 ↗
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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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