Skip to content

Medline Industries, Inc. DYNJ902025Recalls & reported problems

Medline Industries, Inc. · LEX NEURO ANGIOGRAPHY · Class 1

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
2
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10888277888913), received between Mar 9, 2026 and Jun 30, 2026 — classified as 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 18, 2026.

Reports received per month

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 1 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 1 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520261
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Break1
  • Material Separation1

Patient problems

  • No Clinical Signs, Symptoms or Conditions2

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • MalfunctionJun 30, 2026Material Separation

    IT WAS REPORTED THAT THE TOWELS ARE SHEDDING.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 25670002 ↗
  • MalfunctionMar 9, 2026Break

    ACCORDING TO THE CUSTOMER CONTACT ON (B)(6) 2026, SYRINGE BROKE WHILE USING. CUSTOMER CONTACT REPORTED, "SYRINGE BROKE INTO SEVERAL PIECES" AND "SYRINGE WAS BEING USED TO INJECT ½ CONTRAST, ½ SALINE INTO CATHETER".

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 24546053 ↗

Other Neurological tray devices

All Neurological tray devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page