Medline Industries, Inc. VASC1446Recalls & reported problems
Medline Industries, Inc. · LHK AUGUSTA HEALTH CARE · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 9
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 9 adverse event reports that list this exact device (DI 10195327473181), received between Apr 17, 2024 and Sep 29, 2026 — classified as 9 malfunctions.
The most frequently reported specific device problem is “Connection Problem” (7 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 18, 2026.
Reports received per month
Most reported problems
Device problems
- Connection Problem7
- Decoupling2
- Loose or Intermittent Connection1
Patient problems
- Insufficient Information6
- No Clinical Signs, Symptoms or Conditions3
Recent adverse event reports
The 9 most recent of 9 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 29, 2026Decoupling
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50935943 ↗MalfunctionSep 28, 2026Decoupling; Loose or Intermittent Connection
It was reported that "the manifold and syringe backing off when connecting."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50915042 ↗MalfunctionApr 17, 2024Connection Problem; Connection Problem
ACCORDING TO THE CUSTOMER ON 3/8, "DURING A CORONARY ANGIOGRAPHY THE STAFF HAD TO MANUALLY HOLD A SYRINGE IN PLACE FOR THE FINAL FEW INJECTIONS".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19126833 ↗MalfunctionApr 17, 2024Connection Problem; Connection Problem
ACCORDING TO THE CUSTOMER, "IT REALLY DOES SEEM TO BE A MIXTURE OF PRE-PROCEDURE AND MIDDLE OF THE PROCEDURE OCCURRENCES OF THE SAME ISSUE HAPPENING WHERE THE SYRINGE WILL NOT STAY ON THE MANIFOLD WITHOUT PHYSICALLY BEING HELD IN PLACE".
Patient problems: Insufficient Information
MAUDE report 19126425 ↗MalfunctionApr 17, 2024Connection Problem; Connection Problem
ACCORDING TO THE CUSTOMER, "IT REALLY DOES SEEM TO BE A MIXTURE OF PRE-PROCEDURE AND MIDDLE OF THE PROCEDURE OCCURRENCES OF THE SAME ISSUE HAPPENING WHERE THE SYRINGE WILL NOT STAY ON THE MANIFOLD WITHOUT PHYSICALLY BEING HELD IN PLACE".
Patient problems: Insufficient Information
MAUDE report 19126207 ↗MalfunctionApr 17, 2024Connection Problem; Connection Problem
ACCORDING TO THE CUSTOMER, "IT REALLY DOES SEEM TO BE A MIXTURE OF PRE-PROCEDURE AND MIDDLE OF THE PROCEDURE OCCURRENCES OF THE SAME ISSUE HAPPENING WHERE THE SYRINGE WILL NOT STAY ON THE MANIFOLD WITHOUT PHYSICALLY BEING HELD IN PLACE."
Patient problems: Insufficient Information
MAUDE report 19125764 ↗MalfunctionApr 17, 2024Connection Problem; Connection Problem
ACCORDING TO THE CUSTOMER, "IT REALLY DOES SEEM TO BE A MIXTURE OF PRE-PROCEDURE AND MIDDLE OF THE PROCEDURE OCCURRENCES OF THE SAME ISSUE HAPPENING WHERE THE SYRINGE WILL NOT STAY ON THE MANIFOLD WITHOUT PHYSICALLY BEING HELD IN PLACE".
Patient problems: Insufficient Information
MAUDE report 19125515 ↗MalfunctionApr 17, 2024Connection Problem; Connection Problem
ACCORDING TO THE CUSTOMER, "IT REALLY DOES SEEM TO BE A MIXTURE OF PRE-PROCEDURE AND MIDDLE OF THE PROCEDURE OCCURRENCES OF THE SAME ISSUE HAPPENING WHERE THE SYRINGE WILL NOT STAY ON THE MANIFOLD WITHOUT PHYSICALLY BEING HELD IN PLACE".
Patient problems: Insufficient Information
MAUDE report 19125310 ↗MalfunctionApr 17, 2024Connection Problem; Connection Problem
ACCORDING TO THE CUSTOMER, "IT REALLY DOES SEEM TO BE A MIXTURE OF PRE-PROCEDURE AND MIDDLE OF THE PROCEDURE OCCURRENCES OF THE SAME ISSUE HAPPENING WHERE THE SYRINGE WILL NOT STAY ON THE MANIFOLD WITHOUT PHYSICALLY BEING HELD IN PLACE".
Patient problems: Insufficient Information
MAUDE report 19125150 ↗
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- Medline Industries, Inc. ECVC5540ACenturion Medical Products Corporation · Cardiac catheterization kit3 recalls0 reports
- Medline Industries, Inc. ECVC2745Centurion Medical Products Corporation · Cardiac catheterization kit3 recalls0 reports
- Medline Industries, Inc. ECVC6505Centurion Medical Products Corporation · Cardiac catheterization kit3 recalls0 reports
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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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