Medline DYNA22100Recalls & reported problems
Medline Industries, Inc. · CATHETER, IV, SURESITE AUTO, 22G X 1.00" · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 7
- Deaths reported
- 0
- Injuries reported
- 4
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI 10193489140071), received between Jan 2, 2024 and Sep 27, 2026 — classified as 4 injuries, 3 malfunctions.
The most frequently reported specific device problem is “Activation Failure” (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
- Activation Failure1
- Break1
- Expulsion1
- Improper or Incorrect Procedure or Method1
- Key or Button Unresponsive/not Working1
- Material Integrity Problem1
- Material Separation1
- Retraction Problem1
Patient problems
- Foreign Body In Patient3
- No Clinical Signs, Symptoms or Conditions3
- Unintended Loss of Vascular Access1
Recent adverse event reports
The 7 most recent of 7 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 27, 2026Retraction Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50909479 ↗MalfunctionSep 24, 2026Activation Failure; Key or Button Unresponsive/not Working
It was reported that "she withdrew the needle by pressing the button to retract the needle, but didn¿t notice that the button didn¿t work".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50882180 ↗MalfunctionSep 23, 2026Improper or Incorrect Procedure or Method; Expulsion
It was reported that "It would automatically come out of the patient's arm. Catheter would come out and it was tapped down with Tegaderm."
Patient problems: Unintended Loss of Vascular Access
MAUDE report 50866467 ↗InjuryMay 14, 2024Break; Break
ACCORDING TO THE CUSTOMER, ON (B)(6) 2024 THE IV WAS PLACED AND BEING FLUSHED FOR A "COLONOSCOPY" WHEN "THE CATHETER BROKE APART FROM THE HUB INSIDE THE PATIENT".
Patient problems: Foreign Body In Patient
MAUDE report 19311176 ↗InjuryApr 29, 2024Material Separation; Material Separation
THERE WAS A REPORTED INCIDENT WHERE THE CATHETER BECAME DISCONNECTED FROM THE HUB. THE IV NURSE PLACED THE CATHETER AND CONNECTED THE SALINE TO THE SYRINGE TO FLUSH THE LINE AND THE CATHETER DISCONNECTED FROM THE HUB. EMS WAS CALLED DUE TO NURSES BEING UNABLE TO FEEL THE CATHETER.
Patient problems: Foreign Body In Patient
MAUDE report 19202591 ↗InjuryApr 19, 2024
A 50 YO (YEAR-OLD) MALE SCHEDULED FOR A COLONOSCOPY. PATIENT HAD A MEDLINE 22G ANGIOCATH PLACED IN THE RIGHT ANTECUBITAL. NURSE WAS IN THE PROCESS OF FLUSHING SALINE AND THE CATHETER DISLODGED FROM THE BLUE HUB.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19152314 ↗InjuryJan 2, 2024Material Integrity Problem; Material Integrity Problem
IV CATHETER BROKE OFF INTO THE PATIENT.
Patient problems: Foreign Body In Patient
MAUDE report 18426914 ↗
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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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