Medline Industries, Inc. VASC1662Recalls & reported problems
Medline Industries, Inc. · LHK, US, WESTSIDE REGIONAL MED · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 10198459222191), received between Sep 11, 2025 and Sep 12, 2025 — classified as 4 malfunctions.
The most frequently reported specific device problem is “Loose or Intermittent Connection” (4 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
- Loose or Intermittent Connection4
Patient problems
- No Clinical Signs, Symptoms or Conditions4
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 12, 2025Loose or Intermittent Connection; Loose or Intermittent Connection
IT WAS REPORTED THAT THE CONTROL SYRINGE IS "UNRAVELING OFF THE MANIFOLD".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23039539 ↗MalfunctionSep 12, 2025Loose or Intermittent Connection; Loose or Intermittent Connection
IT WAS REPORTED THAT THE CONTROL SYRINGE IS "UNRAVELING OFF THE MANIFOLD".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23039534 ↗MalfunctionSep 11, 2025Loose or Intermittent Connection; Loose or Intermittent Connection
IT WAS REPORTED THAT THE CONTROL SYRINGE IS "UNRAVELING OFF THE MANIFOLD".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23032212 ↗MalfunctionSep 11, 2025Loose or Intermittent Connection; Loose or Intermittent Connection
IT WAS REPORTED THAT THE CONTROL SYRINGE IS "UNRAVELING OFF THE MANIFOLD".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23032187 ↗
Other Cardiac catheterization kit devices
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- Medline Industries, Inc. DYNJ0578916XMedline Industries, Inc. · Cardiac catheterization kit3 recalls0 reports
- Medline Industries, Inc. MNS9935Medline Industries, Inc. · Cardiac catheterization kit3 recalls0 reports
- 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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