Medline Industries, Inc. DYNJRA0496ARecalls & reported problems
Medline Industries, Inc. · UNIVERSAL BLOCK TRAY-LF · Class 2
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 10198459137259), received between Mar 2, 2026 and Sep 8, 2026 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Failure to Align” (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
Most reported problems
Device problems
- Failure to Align1
- Fluid/Blood Leak1
- Obstruction of Flow1
Patient problems
- Insufficient Information1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 8, 2026Failure to Align
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50675124 ↗MalfunctionMar 2, 2026Fluid/Blood Leak; Obstruction of Flow
ACCORDING TO THE CUSTOMER, THE 10 CC SYRINGE FEELS CLOGGED, MEANING YOU CANNOT PUSH IT DOWN WITHOUT CAUSING LEAKING FROM THE PLUNGER.
Patient problems: Insufficient Information
MAUDE report 24484133 ↗
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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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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